LOCUS       NC_000017              19149 bp    DNA     linear   CON 26-MAR-2018
DEFINITION  Homo sapiens chromosome 17, GRCh38.p12 Primary Assembly.
ACCESSION   NC_000017 REGION: complement(7668402..7687550)
VERSION     NC_000017.11
DBLINK      BioProject: PRJNA168
            Assembly: GCF_000001405.38
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 19149)
  AUTHORS   Zody,M.C., Garber,M., Adams,D.J., Sharpe,T., Harrow,J.,
            Lupski,J.R., Nicholson,C., Searle,S.M., Wilming,L., Young,S.K.,
            Abouelleil,A., Allen,N.R., Bi,W., Bloom,T., Borowsky,M.L.,
            Bugalter,B.E., Butler,J., Chang,J.L., Chen,C.K., Cook,A., Corum,B.,
            Cuomo,C.A., de Jong,P.J., DeCaprio,D., Dewar,K., FitzGerald,M.,
            Gilbert,J., Gibson,R., Gnerre,S., Goldstein,S., Grafham,D.V.,
            Grocock,R., Hafez,N., Hagopian,D.S., Hart,E., Norman,C.H.,
            Humphray,S., Jaffe,D.B., Jones,M., Kamal,M., Khodiyar,V.K.,
            LaButti,K., Laird,G., Lehoczky,J., Liu,X., Lokyitsang,T.,
            Loveland,J., Lui,A., Macdonald,P., Major,J.E., Matthews,L.,
            Mauceli,E., McCarroll,S.A., Mihalev,A.H., Mudge,J., Nguyen,C.,
            Nicol,R., O'Leary,S.B., Osoegawa,K., Schwartz,D.C., Shaw-Smith,C.,
            Stankiewicz,P., Steward,C., Swarbreck,D., Venkataraman,V.,
            Whittaker,C.A., Yang,X., Zimmer,A.R., Bradley,A., Hubbard,T.,
            Birren,B.W., Rogers,J., Lander,E.S. and Nusbaum,C.
  TITLE     DNA sequence of human chromosome 17 and analysis of rearrangement
            in the human lineage
  JOURNAL   Nature 440 (7087), 1045-1049 (2006)
   PUBMED   16625196
REFERENCE   2  (bases 1 to 19149)
  CONSRTM   International Human Genome Sequencing Consortium
  TITLE     Finishing the euchromatic sequence of the human genome
  JOURNAL   Nature 431 (7011), 931-945 (2004)
   PUBMED   15496913
REFERENCE   3  (bases 1 to 19149)
  AUTHORS   Lander,E.S., Linton,L.M., Birren,B., Nusbaum,C., Zody,M.C.,
            Baldwin,J., Devon,K., Dewar,K., Doyle,M., FitzHugh,W., Funke,R.,
            Gage,D., Harris,K., Heaford,A., Howland,J., Kann,L., Lehoczky,J.,
            LeVine,R., McEwan,P., McKernan,K., Meldrim,J., Mesirov,J.P.,
            Miranda,C., Morris,W., Naylor,J., Raymond,C., Rosetti,M.,
            Santos,R., Sheridan,A., Sougnez,C., Stange-Thomann,N.,
            Stojanovic,N., Subramanian,A., Wyman,D., Rogers,J., Sulston,J.,
            Ainscough,R., Beck,S., Bentley,D., Burton,J., Clee,C., Carter,N.,
            Coulson,A., Deadman,R., Deloukas,P., Dunham,A., Dunham,I.,
            Durbin,R., French,L., Grafham,D., Gregory,S., Hubbard,T.,
            Humphray,S., Hunt,A., Jones,M., Lloyd,C., McMurray,A., Matthews,L.,
            Mercer,S., Milne,S., Mullikin,J.C., Mungall,A., Plumb,R., Ross,M.,
            Shownkeen,R., Sims,S., Waterston,R.H., Wilson,R.K., Hillier,L.W.,
            McPherson,J.D., Marra,M.A., Mardis,E.R., Fulton,L.A.,
            Chinwalla,A.T., Pepin,K.H., Gish,W.R., Chissoe,S.L., Wendl,M.C.,
            Delehaunty,K.D., Miner,T.L., Delehaunty,A., Kramer,J.B., Cook,L.L.,
            Fulton,R.S., Johnson,D.L., Minx,P.J., Clifton,S.W., Hawkins,T.,
            Branscomb,E., Predki,P., Richardson,P., Wenning,S., Slezak,T.,
            Doggett,N., Cheng,J.F., Olsen,A., Lucas,S., Elkin,C.,
            Uberbacher,E., Frazier,M., Gibbs,R.A., Muzny,D.M., Scherer,S.E.,
            Bouck,J.B., Sodergren,E.J., Worley,K.C., Rives,C.M., Gorrell,J.H.,
            Metzker,M.L., Naylor,S.L., Kucherlapati,R.S., Nelson,D.L.,
            Weinstock,G.M., Sakaki,Y., Fujiyama,A., Hattori,M., Yada,T.,
            Toyoda,A., Itoh,T., Kawagoe,C., Watanabe,H., Totoki,Y., Taylor,T.,
            Weissenbach,J., Heilig,R., Saurin,W., Artiguenave,F., Brottier,P.,
            Bruls,T., Pelletier,E., Robert,C., Wincker,P., Smith,D.R.,
            Doucette-Stamm,L., Rubenfield,M., Weinstock,K., Lee,H.M.,
            Dubois,J., Rosenthal,A., Platzer,M., Nyakatura,G., Taudien,S.,
            Rump,A., Yang,H., Yu,J., Wang,J., Huang,G., Gu,J., Hood,L.,
            Rowen,L., Madan,A., Qin,S., Davis,R.W., Federspiel,N.A.,
            Abola,A.P., Proctor,M.J., Myers,R.M., Schmutz,J., Dickson,M.,
            Grimwood,J., Cox,D.R., Olson,M.V., Kaul,R., Raymond,C., Shimizu,N.,
            Kawasaki,K., Minoshima,S., Evans,G.A., Athanasiou,M., Schultz,R.,
            Roe,B.A., Chen,F., Pan,H., Ramser,J., Lehrach,H., Reinhardt,R.,
            McCombie,W.R., de la Bastide,M., Dedhia,N., Blocker,H.,
            Hornischer,K., Nordsiek,G., Agarwala,R., Aravind,L., Bailey,J.A.,
            Bateman,A., Batzoglou,S., Birney,E., Bork,P., Brown,D.G.,
            Burge,C.B., Cerutti,L., Chen,H.C., Church,D., Clamp,M.,
            Copley,R.R., Doerks,T., Eddy,S.R., Eichler,E.E., Furey,T.S.,
            Galagan,J., Gilbert,J.G., Harmon,C., Hayashizaki,Y., Haussler,D.,
            Hermjakob,H., Hokamp,K., Jang,W., Johnson,L.S., Jones,T.A.,
            Kasif,S., Kaspryzk,A., Kennedy,S., Kent,W.J., Kitts,P.,
            Koonin,E.V., Korf,I., Kulp,D., Lancet,D., Lowe,T.M., McLysaght,A.,
            Mikkelsen,T., Moran,J.V., Mulder,N., Pollara,V.J., Ponting,C.P.,
            Schuler,G., Schultz,J., Slater,G., Smit,A.F., Stupka,E.,
            Szustakowski,J., Thierry-Mieg,D., Thierry-Mieg,J., Wagner,L.,
            Wallis,J., Wheeler,R., Williams,A., Wolf,Y.I., Wolfe,K.H.,
            Yang,S.P., Yeh,R.F., Collins,F., Guyer,M.S., Peterson,J.,
            Felsenfeld,A., Wetterstrand,K.A., Patrinos,A., Morgan,M.J., de
            Jong,P., Catanese,J.J., Osoegawa,K., Shizuya,H., Choi,S. and
            Chen,Y.J.
  CONSRTM   International Human Genome Sequencing Consortium
  TITLE     Initial sequencing and analysis of the human genome
  JOURNAL   Nature 409 (6822), 860-921 (2001)
   PUBMED   11237011
  REMARK    Erratum:[Nature 2001 Aug 2;412(6846):565]
COMMENT     REFSEQ INFORMATION: The reference sequence is identical to
            CM000679.2.
            On Feb 3, 2014 this sequence version replaced NC_000017.10.
            Assembly Name: GRCh38.p12 Primary Assembly
            The DNA sequence is composed of genomic sequence, primarily
            finished clones that were sequenced as part of the Human Genome
            Project. PCR products and WGS shotgun sequence have been added
            where necessary to fill gaps or correct errors. All such additions
            are manually curated by GRC staff. For more information see:
            https://genomereference.org.
            
            ##Genome-Annotation-Data-START##
            Annotation Provider         :: NCBI
            Annotation Status           :: Full annotation
            Annotation Name             :: Homo sapiens Annotation Release 109
            Annotation Version          :: 109
            Annotation Pipeline         :: NCBI eukaryotic genome annotation
                                           pipeline
            Annotation Software Version :: 8.0
            Annotation Method           :: Best-placed RefSeq; Gnomon
            Features Annotated          :: Gene; mRNA; CDS; ncRNA
            ##Genome-Annotation-Data-END##
FEATURES             Location/Qualifiers
     source          1..19149
                     /organism="Homo sapiens"
                     /mol_type="genomic DNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
     gene            complement(<1..1480)
                     /gene="WRAP53"
                     /gene_synonym="DKCB3; TCAB1; WDR79"
                     /note="WD repeat containing antisense to TP53; Derived by
                     automated computational analysis using gene prediction
                     method: BestRefSeq,Gnomon."
                     /db_xref="GeneID:55135"
                     /db_xref="HGNC:HGNC:25522"
                     /db_xref="MIM:612661"
     mRNA            complement(<1327..1480)
                     /gene="WRAP53"
                     /gene_synonym="DKCB3; TCAB1; WDR79"
                     /product="WD repeat containing antisense to TP53,
                     transcript variant 2"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001143990.1"
                     /db_xref="GeneID:55135"
                     /db_xref="HGNC:HGNC:25522"
                     /db_xref="MIM:612661"
     mRNA            complement(<1..111)
                     /gene="WRAP53"
                     /gene_synonym="DKCB3; TCAB1; WDR79"
                     /product="WD repeat containing antisense to TP53,
                     transcript variant 3"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001143991.1"
                     /db_xref="GeneID:55135"
                     /db_xref="HGNC:HGNC:25522"
                     /db_xref="MIM:612661"
     gene            1..19149
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="tumor protein p53; Derived by automated
                     computational analysis using gene prediction method:
                     BestRefSeq."
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10932..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 2"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126112.2"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10932..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 2"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276761.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 1"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_000546.5"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 1"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276760.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14285..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 4"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126113.2"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14285..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 4"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276695.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14212..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 3"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126114.2"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11030,11148..11169,11279..11557,
                     12315..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14212..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 3"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276696.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(1..174,10929..11169,11279..11557,12315..12498,
                     12580..12692,13261..13370,13714..13850,13943..14016,
                     16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 8"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126118.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     CDS             join(10957..11030,11148..11169,11279..11557,12315..12498,
                     12580..12692,13261..13370,13714..13850,13943..14016,
                     16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform a is encoded by transcript variant 1;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform a"
                     /protein_id="NP_000537.3"
                     /db_xref="CCDS:CCDS11118.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLM
                     LSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKT
                     YQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAM
                     AIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVV
                     PYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCA
                     CPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRG
                     RERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDS
                     D"
     CDS             join(10957..11030,11148..11169,11279..11557,12315..12498,
                     12580..12692,13261..13370,13714..13850,13943..14016,
                     16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform a is encoded by transcript variant 2;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform a"
                     /protein_id="NP_001119584.1"
                     /db_xref="CCDS:CCDS11118.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLM
                     LSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKT
                     YQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAM
                     AIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVV
                     PYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCA
                     CPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRG
                     RERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDS
                     D"
     CDS             join(10957..11030,11148..11169,11279..11557,12315..12498,
                     12580..12692,13261..13370,13714..13850,13943..14016,
                     14285..14332)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform c is encoded by transcript variant 4;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform c"
                     /protein_id="NP_001119585.1"
                     /db_xref="CCDS:CCDS45605.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLM
                     LSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKT
                     YQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAM
                     AIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVV
                     PYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCA
                     CPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQMLL
                     DLRWCYFLINSS"
     CDS             join(10957..11030,11148..11169,11279..11557,12315..12498,
                     12580..12692,13261..13370,13714..13850,13943..14016,
                     14212..14244)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform b is encoded by transcript variant 3;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform b"
                     /protein_id="NP_001119586.1"
                     /db_xref="CCDS:CCDS45606.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLM
                     LSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKT
                     YQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAM
                     AIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVV
                     PYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCA
                     CPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQDQT
                     SFQKENC"
     CDS             join(11300..11557,12315..12498,12580..12692,13261..13370,
                     13714..13850,13943..14016,16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform g is encoded by transcript variant 8;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform g"
                     /protein_id="NP_001119590.1"
                     /db_xref="CCDS:CCDS73969.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MDDLMLSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPA
                     APAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTC
                     PVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEG
                     NLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITL
                     EDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSS
                     PQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKK
                     GQSTSRHKKLMFKTEGPDSD"
     CDS             join(11300..11557,12315..12498,12580..12692,13261..13370,
                     13714..13850,13943..14016,16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform g is encoded by transcript variant 1;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform g"
                     /protein_id="NP_001263689.1"
                     /db_xref="CCDS:CCDS73969.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MDDLMLSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPA
                     APAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTC
                     PVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEG
                     NLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITL
                     EDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSS
                     PQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKK
                     GQSTSRHKKLMFKTEGPDSD"
     CDS             join(11300..11557,12315..12498,12580..12692,13261..13370,
                     13714..13850,13943..14016,16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform g is encoded by transcript variant 2;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform g"
                     /protein_id="NP_001263690.1"
                     /db_xref="CCDS:CCDS73969.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MDDLMLSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPA
                     APAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTC
                     PVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEG
                     NLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITL
                     EDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSS
                     PQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKK
                     GQSTSRHKKLMFKTEGPDSD"
     CDS             join(11300..11557,12315..12498,12580..12692,13261..13370,
                     13714..13850,13943..14016,14285..14332)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform h is encoded by transcript variant 4;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform h"
                     /protein_id="NP_001263624.1"
                     /db_xref="CCDS:CCDS73970.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MDDLMLSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPA
                     APAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTC
                     PVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEG
                     NLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITL
                     EDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSS
                     PQPKKKPLDGEYFTLQMLLDLRWCYFLINSS"
     CDS             join(11300..11557,12315..12498,12580..12692,13261..13370,
                     13714..13850,13943..14016,14212..14244)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform i is encoded by transcript variant 3;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform i"
                     /protein_id="NP_001263625.1"
                     /db_xref="CCDS:CCDS73971.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MDDLMLSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPA
                     APAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTC
                     PVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEG
                     NLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITL
                     EDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSS
                     PQPKKKPLDGEYFTLQDQTSFQKENC"
     mRNA            join(12058..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 5"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126115.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(12058..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 5"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276697.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(12058..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14285..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 7"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126117.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(12058..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14285..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 7"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276699.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(12058..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14212..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 6"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001126116.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     mRNA            join(12058..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14212..14344,16836..16942,17861..19149)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /product="tumor protein p53, transcript variant 6"
                     /note="Derived by automated computational analysis using
                     gene prediction method: BestRefSeq."
                     /transcript_id="NM_001276698.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
     CDS             join(12336..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform d is encoded by transcript variant 5;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform d"
                     /protein_id="NP_001119587.1"
                     /db_xref="CCDS:CCDS73966.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRC
                     PHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHY
                     NYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKK
                     GEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALEL
                     KDAQAGKEPGGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD"
     CDS             join(12336..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14285..14332)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform f is encoded by transcript variant 7;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform f"
                     /protein_id="NP_001119589.1"
                     /db_xref="CCDS:CCDS73967.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRC
                     PHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHY
                     NYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKK
                     GEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQMLLDLRWCYFLINSS"
     CDS             join(12336..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14212..14244)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform e is encoded by transcript variant 6;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform e"
                     /protein_id="NP_001119588.1"
                     /db_xref="CCDS:CCDS73968.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRC
                     PHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHY
                     NYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKK
                     GEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQDQTSFQKENC"
     CDS             join(12417..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,16836..16942,17861..17942)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform j is encoded by transcript variant 5;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform j"
                     /protein_id="NP_001263626.1"
                     /db_xref="CCDS:CCDS73963.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRV
                     EYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSS
                     GNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPK
                     KKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKKGQST
                     SRHKKLMFKTEGPDSD"
     CDS             join(12417..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14285..14332)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform l is encoded by transcript variant 7;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform l"
                     /protein_id="NP_001263628.1"
                     /db_xref="CCDS:CCDS73964.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRV
                     EYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSS
                     GNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPK
                     KKPLDGEYFTLQMLLDLRWCYFLINSS"
     CDS             join(12417..12498,12580..12692,13261..13370,13714..13850,
                     13943..14016,14212..14244)
                     /gene="TP53"
                     /gene_synonym="BCC7; LFS1; P53; TRP53"
                     /note="isoform k is encoded by transcript variant 6;
                     Derived by automated computational analysis using gene
                     prediction method: BestRefSeq."
                     /codon_start=1
                     /product="cellular tumor antigen p53 isoform k"
                     /protein_id="NP_001263627.1"
                     /db_xref="CCDS:CCDS73965.1"
                     /db_xref="GeneID:7157"
                     /db_xref="HGNC:HGNC:11998"
                     /db_xref="MIM:191170"
                     /translation="MAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRV
                     EYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSS
                     GNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPK
                     KKPLDGEYFTLQDQTSFQKENC"
ORIGIN      
        1 gatgggattg gggttttccc ctcccatgtg ctcaagactg gcgctaaaag ttttgagctt
       61 ctcaaaagtc tagagccacc gtccagggag caggtagctg ctgggctccg gggacacttt
      121 gcgttcgggc tgggagcgtg ctttccacga cggtgacacg cttccctgga ttgggtaagc
      181 tcctgactga acttgatgag tcctctctga gtcacgggct ctcggctccg tgtattttca
      241 gctcgggaaa atcgctgggg ctgggggtgg ggcagtgggg acttagcgag tttgggggtg
      301 agtgggatgg aagcttggct agagggatca tcataggagt tgcattgttg ggagacctgg
      361 gtgtagatga tggggatgtt aggaccatcc gaactcaaag ttgaacgcct aggcagagga
      421 gtggagcttt ggggaacctt gagccggcct aaagcgtact tctttgcaca tccacccggt
      481 gctgggcgta gggaatccct gaaataaaag atgcacaaag cattgaggtc tgagactttt
      541 ggatctcgaa acattgagaa ctcatagctg tatattttag agcccatggc atcctagtga
      601 aaactggggc tccattccga aatgatcatt tgggggtgat ccggggagcc caagctgcta
      661 aggtcccaca acttccggac ctttgtcctt cctggagcga tctttccagg cagcccccgg
      721 ctccgctaga tggagaaaat ccaattgaag gctgtcagtc gtggaagtga gaagtgctaa
      781 accaggggtt tgcccgccag gccgaggagg accgtcgcaa tctgagaggc ccggcagccc
      841 tgttattgtt tggctccaca tttacatttc tgcctcttgc agcagcattt ccggtttctt
      901 tttgccggag cagctcacta ttcacccgat gagaggggag gagagagaga gaaaatgtcc
      961 tttaggccgg ttcctcttac ttggcagagg gaggctgcta ttctccgcct gcatttcttt
     1021 ttctggatta cttagttatg gcctttgcaa aggcaggggt atttgttttg atgcaaacct
     1081 caatccctcc ccttctttga atggtgtgcc ccaccccgcg ggtcgcctgc aacctaggcg
     1141 gacgctacca tggcgtgaga cagggaggga aagaagtgtg cagaaggcaa gcccggaggt
     1201 attttcaaga atgagtatat ctcatcttcc cggaggaaaa aaaaaaagaa tgggtacgtc
     1261 tgagaatcaa attttgaaag agtgcaatga tgggtcgttt gataatttgt cggaaaaaca
     1321 atctacctgt tatctagctt tgggctaggc cattccagtt ccagacgcag gctgaacgtc
     1381 gtgaagcgga aggggcgggc ccgcaggcgt ccgtgtggtc ctccgtgcag ccctccggcc
     1441 cgagccggtt cttcctggta ggaggcggaa ctcgaattca tttctcccgc tgccccatct
     1501 cttagctcgc ggttgtttca ttccgcagtt tcttcccatg cacctgccgc gtaccggcca
     1561 ctttgtgccg tacttacgtc atctttttcc taaatcgagg tggcatttac acacagcgcc
     1621 agtgcacaca gcaagtgcac aggaagatga gttttggccc ctaaccgctc cgtgatgcct
     1681 accaagtcac agaccctttt catcgtccca gaaacgtttc atcacgtctc ttcccagtcg
     1741 attcccgacc ccacctttat tttgatctcc ataaccattt tgcctgttgg agaacttcat
     1801 atagaatgga atcaggctgg gcgctgtggc tcacgcctgc actttgggag gccgaggcgg
     1861 gcggattact tgaggatagg agttccagac cagcgtggcc aacgtggtga atccccgtct
     1921 ctactaaaaa atacaaaaat tagctgggcg tggtgggtgc ctgtaatccc agctattcgg
     1981 gagggtgagg caggagaatc gcttgaaccc gggaggcaga ggttgcagtg agccaagatc
     2041 gtgccactac actccagcct gggcgacaag aacgaaactc cgtctcaaaa aaaagggggg
     2101 aatcatacat tatgtgctca tttttgtcgg gcttctgtcc ttcaatgtac tgtctgacat
     2161 tcgttcatgt tgtatatatc agtattttgc tccttttcat ttagtatagt ccatcgattg
     2221 tatatccgtc cttttgatgg ccttttgagt tgtttcccat ttgcggttat gaaataaagc
     2281 tgctataaac attcttgtac aattcttttt gtgatcatat gttttcgtgt ttcttggaga
     2341 aatacttagg aggggaattg cgagtttgga agtaaaaagt agctgtattt tgaacttttt
     2401 cagaagctct gagttttcca gagcggttgt accattttac actccaacta gcaaggtatg
     2461 ggagttatta tggttgtgcc acagccttcc ggacattagg tattgtcagt ctttctaatg
     2521 tggtatatcc ttgtggttgt aatttacagt tctctattga ctaaggatgt tcagcatttt
     2581 ttcatgtgcc tattggccat tcgtattttg tttgtaaagt agctcttcga gtcttttacc
     2641 tgttattttg gttttttgtt tgtttttatt gttcagttgt gggactgctt tatacattct
     2701 ggatacaagt cctttatcag atccatgtgt cgtgaatgtt ttcttctgat ctgttgcttg
     2761 cctatttgtt tgctttacag agtttacagt atcttaagag gagtggattt atctttttta
     2821 tgttcagtat ttgccttgtc ctgtttagga catctttttt ttttttttta accccagggt
     2881 catgaagata ttatcttaca ttttctttta ggacctttat ggttgtaagt tttacagtaa
     2941 ggtccttgag ccattaatta attcttaaaa ttaattgttt atggtgtgag gtgtaggagt
     3001 cagtctctgg tatctttcct gtatggaaat ccagttattc tgtctccact tgttgaaata
     3061 ggcttccttt ctctactgaa tgcttttaat tttaattatt ttacagttgg agtatagggc
     3121 taccatttta gtgctatttt ctttttttct ttgttaattt ttgagacagg gactcacact
     3181 gttgcccagg ctagagtaca atggcacaat caaggcttac tgcagcctcg aacccctggg
     3241 ctcaagcagt cctctagcag cctcacgagt agctgggatt actccaccac acccagctaa
     3301 ctattttatt tttttgtatt gacaggatct cactatgttg cccaggctgg tctcaaactg
     3361 ctggcctcaa gctttcatcc catctcggcc tcccaaagtg ctgggattac aggtgtgagc
     3421 caccatgcct gacctcttag tgctattttc tatttatctc ctctgttctc tgctctcttt
     3481 aaacgttgga ggaagaaaca gtacccatct tacacaaact cttcagaaaa cagaggaaca
     3541 gactgggcgc ggtggctcat acctgtaatc tcagcacttt ggtacgctga ggcaggggat
     3601 catttgaggt cgggagttcg agaccagcct ggccaacacg gcgaaacccc atctctacta
     3661 aaaatacaaa aagtagctag gcgtggtgac acatacctgt aatgccagtt actcaggagg
     3721 ctgaggcaca agaatccctt gaacctggga agcggaggtt gcagtgagcc gagattgcgc
     3781 cactgcactc cagcctgggc aacagagtga gaccctgtct cagaaaaaaa aagaaagaaa
     3841 gaaaaaatag aggaatattt cccaacttgt tttcgaagcc agcataatcc tggtaccaaa
     3901 accaaacaag gacattataa gaaaagaaaa tatagaccaa tattcctgtt agcatagaca
     3961 tgcaacagct aaccaatttt agcaaaccaa acctggtaat atagaaaaaa ggataaatag
     4021 gccagtcgcg gtggctcacg cctgtaatcc cagcactttg ggaggctgag gcaggcagat
     4081 cacttgaggt caggagtttg agaccagcct gaccaacatg gtgaaacccc gtttctaata
     4141 aaaatacaaa aatcaggctg ggcacggtgg ctcacgcctg taatcccagc actttgggag
     4201 gccgaggtgg gcagatcacg aggtcaggag ttcaagacca gcctgaccaa tgtggtgaaa
     4261 cgccatctct actaaaaata caaaaatcag ccggtgtggt ggcacctgcc tgtaatccca
     4321 gctactcagg aggctgaggc agaattgctt gaacccggga ggcagaggtt gcagtgagcc
     4381 aagatcgtgc cactgcactc cagcctgggc gacagagcaa gacttcatct caaaaaaaaa
     4441 aaaaaattag ctgggcatgg tggtgggcac ctgaaatccc agctactcgg gagtctgagg
     4501 caggagaatc gcttgaaccc aggaggcaga agttgcactg agctgggatc acaccattgc
     4561 actccagcct gggcaacaga gtgagactcc atctcaaaaa aagaaaaaga aaaaggataa
     4621 atacattcta accaaataat gtttatctca tgattgtagc tgattcaaca ttcaaaaatt
     4681 ggcctggtgc agtagctcag gcctgtaatc ccaacatttt aggaggctga ggcaggaaga
     4741 tctcttgagc ccaggatttc aagaccagcc tgggcaacat agtcagactg gtctttactg
     4801 gggggaaaaa aatcagtctg tgtaattcac cacattaaca aagggaaaca taaaaaccct
     4861 atgatcattt caacagatgt agcaaaagca gttaatgata ttcaacacat atgcatgatt
     4921 acaaaccaac caacctccta gcaaactagg gaaaggaaac ttaacctagt ttgataacag
     4981 ggcgtccaca gtcggagttc cactagcagc atacataatg gtagaaaact cagtgctgcc
     5041 gggcgcggtg gctcacgcct gtaatgccag cactttggga ggcctaggcg ggcggatcac
     5101 gaggtcagga gatcgagact gtcctgacta gcatgctgaa accccgtctc tactaaaaat
     5161 acaaaaacaa aaaattagcc gggcatggtg gcgggcgcct atagtcccag ctactcggga
     5221 ggctgaggcg agagaatggc gtgaacccgg gaggcggagc ttgcagagcc tagatcgtgc
     5281 cactgcactc cagcctgggt gacagagtga gacttcgtct caaaaaaaaa aaaaaaaaaa
     5341 aaagaaaaga aaactcaacg ctttttcctc taagatcagg aactagaaaa ggatttgact
     5401 ctcacaacgt tgataccata ctggaggttt taaccaggca agaaaaagaa ataatgaggg
     5461 ccgggtgcgg tggctcaggc ctgtaatccc agcactttgg gaagccgaga cgggtggatc
     5521 acgaggtcag gagatcgaga ccatcctggc taacacggtg aaaccctgtc tctactaaat
     5581 atacaaaaaa ttagccgggc gtagtggcgg gcgcctgtag tcccagctac tcgggaggct
     5641 gaggcaggag aatggcgtga actcaggggg cggagcttgc agtgagctga gatcgagcca
     5701 ctgcactcca gcctgggcga cagagcaaga ctgtgtctca aaaaaaaaaa aagaaaaaga
     5761 aataatgatt agtggcccga tgtctcacgc ctataatccc agcactttgg gaggccgagg
     5821 tgggcagatc acctgaggtc tggagttgga gaccagcctg acaaagatgg tgaaacctcg
     5881 tctctattaa aatattaaaa aaatagccag gcgttggccg ggtacagtgg ctcatgcctg
     5941 taatcccagc actttgggag gccgaggtgg gtggatcacc tgaggtcagg agttcaacac
     6001 cagcctggcc aacatggtga aaccccatct ctactaaaaa tacaaaaatt agccgggcgt
     6061 agtggcgggc gcctgtaatc ccagctactt gggaggctta ggcaggagaa tcgcttgaac
     6121 ctgggaggcg gaggttgtag tgagccgaga ttgcaccatt gcactccagc ctgggtgaca
     6181 aaagcaaaaa ctccgtctca aaaaaaaaag aattagccag gggtagtggt gaacgcctgt
     6241 agtcccagct actcaggagg cagaggcagg agaatcactt gaacccagga ggcagaggtt
     6301 gcagtgagcc gagattgtcc cattgcactc cagcctaggc gacaagagca aaattccatg
     6361 tcaaaaaaaa aaaaaaaaaa ggaaagaaaa aaaataacga ttagaaagga agaaataaaa
     6421 cacattcaca gccagtatga ttctatacat acatgtccta atggggccag gcgtggtggc
     6481 tcatgcctgt aatcctagca cttttaggag gctgaggcag gtggcttccc tgggaccagc
     6541 ctggccaaca tggtgaaacc ccaactctaa taaaaataca aaaaatcagc caggcgtggt
     6601 gacgggcacc tctaatccca gctactcagg aggctgaggc aggagaattg cttggacctg
     6661 ggaggcagag gttgcagtga gccgagatcg cgctattgca ctccagcctg ggcaacaaga
     6721 gtgaaactcc ggcagggtgt ggtggcttac gcctgtaatc ccagcacttc gggaggctga
     6781 ggcaggccga tcacctgagg tcaggagttt gagaccaacc taacatggtg aaaccccgtc
     6841 tctactaaaa atacaagaat tagctgggtg tagtggtggg cgcctgtaat cccagctact
     6901 tgggaggctg agacagaaga attgcttgaa cccaggaggt ggaggttgca gtgagctgag
     6961 atcatgccat tgcacaccac gccgggcaac agagcgagat tccgtctcaa aaaaaaaaaa
     7021 aaagagtgaa actctatctc aaaaaaaaaa aaaagtccta atggaaaatc cataaaaagc
     7081 taccaaaact aataaataaa tatagcaggg ttgcaggtta cagggcaata tagttatccc
     7141 tctatctgta ggggcttggt tctgggactc ctcacacacc aaacccacag atgtctaagt
     7201 cccatatata agacggtata gtatttggat ttaacctaca catatcctcc catatagttt
     7261 aaattatctc tagattactt acattacccc catacaatga aaatgctaat gtacatgcaa
     7321 gtatgtatgt aagtacttgt actatattgt ttagggaatc actggacata taggccttca
     7381 agactgatac cagcagccac tgttaagatt ctggtcaggc ctgcccctgt ttggggtctc
     7441 agttgatctc attgccttcc cacccagcca agggcacctg catttctctt ggctccctgg
     7501 ccatttggaa ggcctagttc agcctggcac atttgtatcc tggcccactg atgctggtac
     7561 ccctgggaag gtcctgctct gaaaaacacg gagattttag ttgctactga agatttgaga
     7621 gataaagaca gggagacctg tctgtagacc tgtgtccctc caagtgggat tgagactttg
     7681 ggccccccat ttcaggacag cacctcctgg cctgttgact gaatagatcc ctgaaggagg
     7741 tgtacttgca ttaatggagt gggggtggga gcagtaccac agatccgcac taacaatcac
     7801 acagttctct ctagaataat aatatagaac aagtgaaata gaacaattgc agaaagagct
     7861 aacctttgtt gagctcttac tgtgtgccca gcactttcct caactctaca tttcccataa
     7921 tacacagagt actaggtagg ccaggcttgg tggctcacgc ctgtaatccc agcactttag
     7981 gaggccaagg ggggtggatc acctgaggtc gggagttcaa gaccagcctg accaacatgg
     8041 tgaaaccccg tctctactag aagtacaaaa ttagccaggt gtggtggcac atgcttgtag
     8101 tcctagctac tcagcaggct gaggcaggag aatcatttga atccgggagg aggttgcagt
     8161 aagcggagat agtgccactg tactccagcc tgggcaataa gagctgagac tccgtctcaa
     8221 aataaaataa aataaaataa aataaaataa aataaaataa aaaaagaaaa gagcctgcca
     8281 ttaaaggagc tgtttggtag gggatgtttt gtcagtgcaa acaacagaaa agtgggctgg
     8341 gcacagtggt tcatgcctgt aatcccagca ctttgggagg ccaaggcggg cggatcacct
     8401 gaagttggga gttcaagacc agcctgacca atatggagaa accccgtctc tactaaaaat
     8461 acaaaattag ccgggcgcag tggcgcatgc ctgtaatccc agctactcgg gaggctgagg
     8521 caggagaatc gcttgaacct gggaggcaga ggttgcggtg agccgagatc gcaccattgc
     8581 actccagcct ggacgagagc aaaactctgt ctcaaaaaaa aaaaaaaaca gaaaagtgta
     8641 acaaacactt acagtaggca tgtttcttag caaatctgat gacaaatttg gcataaagaa
     8701 agagagcatc cctgaaaaaa aaaaaaagaa aaagaaagag agcatcctgc ctgggcaaca
     8761 tagtgaaacc ctgcctctac aaaaaaactc aaaaattggc cgggtgcagt ggctcacacc
     8821 tgtaatccca gcactttggg agtcggaggc gggaggatca cctgaggtca ggagttcgaa
     8881 accagcctgg ccaacatggc aaaaccccat ctctactaaa aatacaaaaa attaatcagg
     8941 cgcattggtg ggcgcctgta atcccagcta ctcaggaagt tgaggcaaga ggatcgcttg
     9001 aatctgggag gtggaggtta cagtgagtcg agatcacacc actgcactct agcctgggtg
     9061 acagggcgag actccgtctc caaaaaaaaa aagaaaaaga aaaagactaa aaaattagcc
     9121 aggcaggcct ctgtggtccc agctacttgg gaggctgagg caggagaatc actgagccca
     9181 ggagtccgag gctgtagtga gccatgattg caccactgta ccctagcttg ggcaacaaag
     9241 caagaccctg cctcaaaaga aaaaagaaag aaagaaagaa catggcgggc caggcacagt
     9301 ggctcacacc tgtaatccca gcgctttgag aggccgaggc aggtggatca caaggtcagg
     9361 agttccacac cagcctggcc aacatggtga aaccctgtct ctactaaaaa tacaaaaaat
     9421 cagccaggca tggtggcagg ggcctgtaat cccagctact cgggaggctg aggcaggaga
     9481 attgcttgaa accagaaggc agaggttgca gtgagcctag actgcaccac tgcactccag
     9541 cctgggcgaa aagagccaaa ctccatctca aaaaacaaac aaaaaaacaa aacaaaagaa
     9601 aacatggcaa agcctttgaa agcttgtctg ggagaaggtg cgatgatagt tgcataactt
     9661 cgtgcaagat gctggtccac acaggggctg ccccttgctc tttctcgctc tcttaacctc
     9721 tcatataaca ggcttgtgtg ttattcacat ttattgagcc caagcaggtg caaggcattg
     9781 tgatctaata ctttggtcag caagacaaca agatagatca ctgccctgcc cttaggaagt
     9841 gtatatgcta ttagaggaaa cagataaaat aaacaaggaa aagtatcaga caatgtaagt
     9901 gctatgagaa tgcaaatgag gtgatgtgaa ttaaaatagg atgacttaaa gtctgcacgg
     9961 gaaggagcct acccccatgt tcctggctag ccaaggaacc accagttgat tagcagagaa
    10021 gggcagccag tctagctaga gcttttgggg aagagggagt ggttgttaag agatgagatt
    10081 aaagaagccg agacgggcca ttcgtgaggg gtttgtaatg cagggctgag gagtgtccga
    10141 agagaatggg caggtgagcg gtgagacagt tgttcttcca gaagctttgc agtgaaagga
    10201 atcaaagaaa tggagccgtg tatcaggtgg ggaagggtgg gggccaaggg ggtgtccttc
    10261 cccatacaga gattgcaggc tgagaatgac tatatccttg ttaacaggag gtgggagcag
    10321 ggcacggtag ctcacacctg taatcttggc actttaggag gctgaggcgg gccgatcacc
    10381 tgaagtaagg agttcgagac cagcctggcc aacatgcaaa gccctgtctc tactaaaaat
    10441 acaaaaatta gctgggtgtg gtggtactcg cctgtaatcc cagctactcg ggagactgag
    10501 gcaggagaat ggcttgaacc cggaaggtag aggttgcagt gagctgagat catgccactg
    10561 tgctccagcc taggtgacag agagagactc catctcaaaa aaaaaaaaaa aatacaggaa
    10621 gggagttggg aatagggtgc acatttagga agtcttgggg atttagtggt gggaaggttg
    10681 gaagtccctc tctgattgtc ttttcctcaa agaagtgcat ggctggtgag gggtggggca
    10741 ggagtgcttg ggttgtggtg aaacattgga agagagaatg tgaagcagcc attcttttcc
    10801 tgctccacag gaagccgagc tgtctcagac actggcatgg tgttggggga gggggttcct
    10861 tctctgcagg cccaggtgac ccagggttgg aagtgtctca tgctggatcc ccacttttcc
    10921 tcttgcagca gccagactgc cttccgggtc actgccatgg aggagccgca gtcagatcct
    10981 agcgtcgagc cccctctgag tcaggaaaca ttttcagacc tatggaaact gtgagtggat
    11041 ccattggaag ggcaggccca ccacccccac cccaacccca gccccctagc agagacctgt
    11101 gggaagcgaa aattccatgg gactgacttt ctgctcttgt ctttcagact tcctgaaaac
    11161 aacgttctgg taaggacaag ggttgggctg gggacctgga gggctgggga cctggagggc
    11221 tggggggctg gggggctgag gacctggtcc tctgactgct cttttcaccc atctacagtc
    11281 ccccttgccg tcccaagcaa tggatgattt gatgctgtcc ccggacgata ttgaacaatg
    11341 gttcactgaa gacccaggtc cagatgaagc tcccagaatg ccagaggctg ctccccccgt
    11401 ggcccctgca ccagcagctc ctacaccggc ggcccctgca ccagccccct cctggcccct
    11461 gtcatcttct gtcccttccc agaaaaccta ccagggcagc tacggtttcc gtctgggctt
    11521 cttgcattct gggacagcca agtctgtgac ttgcacggtc agttgccctg aggggctggc
    11581 ttccatgaga cttcaatgcc tggccgtatc cccctgcatt tcttttgttt ggaactttgg
    11641 gattcctctt caccctttgg cttcctgtca gtgttttttt atagtttacc cacttaatgt
    11701 gtgatctctg actcctgtcc caaagttgaa tattcccccc ttgaatttgg gcttttatcc
    11761 atcccatcac accctcagca tctctcctgg ggatgcagaa cttttctttt tcttcatcca
    11821 cgtgtattcc ttggcttttg aaaataagct cctgaccagg cttggtggct cacacctgca
    11881 atcccagcac tctcaaagag gccaaggcag gcagatcacc tgagcccagg agttcaagac
    11941 cagcctgggt aacatgatga aacctcgtct ctacaaaaaa atacaaaaaa ttagccaggc
    12001 atggtggtgc acacctatag tcccagccac ttaggaggct gaggtgggaa gatcacttga
    12061 ggccaggaga tggaggctgc agtgagctgt gatcacacca ctgtgctcca gcctgagtga
    12121 cagagcaaga ccctatctca aaaaaaaaaa aaaaaaagaa aagctcctga ggtgtagacg
    12181 ccaactctct ctagctcgct agtgggttgc aggaggtgct tacgcatgtt tgtttctttg
    12241 ctgccgtctt ccagttgctt tatctgttca cttgtgccct gactttcaac tctgtctcct
    12301 tcctcttcct acagtactcc cctgccctca acaagatgtt ttgccaactg gccaagacct
    12361 gccctgtgca gctgtgggtt gattccacac ccccgcccgg cacccgcgtc cgcgccatgg
    12421 ccatctacaa gcagtcacag cacatgacgg aggttgtgag gcgctgcccc caccatgagc
    12481 gctgctcaga tagcgatggt gagcagctgg ggctggagag acgacagggc tggttgccca
    12541 gggtccccag gcctctgatt cctcactgat tgctcttagg tctggcccct cctcagcatc
    12601 ttatccgagt ggaaggaaat ttgcgtgtgg agtatttgga tgacagaaac acttttcgac
    12661 atagtgtggt ggtgccctat gagccgcctg aggtctggtt tgcaactggg gtctctggga
    12721 ggaggggtta agggtggttg tcagtggccc tccaggtgag cagtaggggg gctttctcct
    12781 gctgcttatt tgacctccct ataaccccat gagatgtgca aagtaaatgg gtttaactat
    12841 tgcacagttg aaaaaactga agcttacaga ggctaagggc ctcccctgct tggctgggcg
    12901 cagtggctca tgcctgtaat cccagcactt tgggaggcca aggcaggcgg atcacgaggt
    12961 tgggagatcg agaccatcct ggctaacggt gaaaccccgt ctctactgaa aaatacaaaa
    13021 aaaaattagc cgggcgtggt gctgggcacc tgtagtccca gctactcggg aggctgagga
    13081 aggagaatgg cgtgaacctg ggcggtggag cttgcagtga gctgagatca cgccactgca
    13141 ctccagcctg ggcgacagag cgagattcca tctcaaaaaa aaaaaaaaaa ggcctcccct
    13201 gcttgccaca ggtctcccca aggcgcactg gcctcatctt gggcctgtgt tatctcctag
    13261 gttggctctg actgtaccac catccactac aactacatgt gtaacagttc ctgcatgggc
    13321 ggcatgaacc ggaggcccat cctcaccatc atcacactgg aagactccag gtcaggagcc
    13381 acttgccacc ctgcacactg gcctgctgtg ccccagcctc tgcttgcctc tgacccctgg
    13441 gcccacctct taccgatttc ttccatacta ctacccatcc acctctcatc acatccccgg
    13501 cggggaatct ccttactgct cccactcagt tttcttttct ctggctttgg gacctcttaa
    13561 cctgtggctt ctcctccacc tacctggagc tggagcttag gctccagaaa ggacaagggt
    13621 ggttgggagt agatggagcc tggtttttta aatgggacag gtaggacctg atttccttac
    13681 tgcctcttgc ttctcttttc ctatcctgag tagtggtaat ctactgggac ggaacagctt
    13741 tgaggtgcgt gtttgtgcct gtcctgggag agaccggcgc acagaggaag agaatctccg
    13801 caagaaaggg gagcctcacc acgagctgcc cccagggagc actaagcgag gtaagcaagc
    13861 aggacaagaa gcggtggagg agaccaaggg tgcagttatg cctcagattc acttttatca
    13921 cctttccttg cctctttcct agcactgccc aacaacacca gctcctctcc ccagccaaag
    13981 aagaaaccac tggatggaga atatttcacc cttcaggtac taagtcttgg gacctcttat
    14041 caagtggaaa gtttccagtc taacactcaa aatgccgttt tcttcttgac tgttttacct
    14101 gcaattgggg catttgccat cagggggcag tgatgcctca aagacaatgg ctcctggttg
    14161 tagctaacta acttcagaac accaacttat accataatat atattttaaa ggaccagacc
    14221 agctttcaaa aagaaaattg ttaaagagag catgaaaatg gttctatgac tttgcctgat
    14281 acagatgcta cttgacttac gatggtgtta cttcctgata aactcgtcgt aagttgaaaa
    14341 tattgtaagt tgaaaatgga tttaatacac ctaatctaag gaacatcata gcttagccta
    14401 gcctgctttt tttttttttt tttttggaga cagagtctca ctctgtcacc caggctggag
    14461 tgcagtggcg ggatctcggc tcactgcaac ctccgccttc tgggttcaag cgattctcct
    14521 gcctcagccc actgagtagc tgggattaca ggcacctgcc ccgacgccca gctaattttt
    14581 tgttatttat ttattttttt ttttagtaga gatgaggttt caccatgttg gccaggctag
    14641 tctcgaactc ctgaccttgt gatctgcctg ccttggcctc ccaaagtgct gggattacag
    14701 gcgtgagcca ccgcacccgg cctgcctagc ctacttttat tttattttta atggagacag
    14761 catcttgctc tgttgcccag gctggattac agtgatgtga tcatagctca ttataccctc
    14821 ctgggctcaa gcaatccccc taactctgcc tccccagtag ctaggaccac aggcatacac
    14881 caccataccc agctaatttt taaaattttt tgtagataga tagagtctca ctatgttgcc
    14941 caggctggtc tctagcctac ttttttgaga caaggtcttg ctctgtcacc caggctggat
    15001 agagtgcagt agtgcagtca cagctcactg cagcctccac ctcccaggct ccatccatcc
    15061 tcccagctca gcctcccaag ttgcttcaac tacaggcctg caccaccatg cctggctaat
    15121 ttttatttat ttatttttat tttattttat tttatttttt tgagactcag tctcactctg
    15181 tcgcccaggc tggagtgcag tggcatgatc tcggctcact gcaacctctg cctcctgggt
    15241 tcaagtgatt ctcctgcctc agcctcccga atagctagga ctacaagcgc ctgctaccac
    15301 gcccagctaa tttttgtatt tttagtagag acagggtttc accatgttgg ccaggctggt
    15361 ctcgaacttc tgaccatgtg atccgcccgc ctcggcctcc caaagtgctg ggattacagg
    15421 tgtgagccac cacgcccggc taatttttat ttatttattt aaagacagag tctcactctg
    15481 tcactcaggc tagagtgcag tggcaccatc tcagctcact gcagccttga cctccctggg
    15541 ctccggtgat ttcaccctcc caagtagcta ggactacagg cacatgccac gacacccagc
    15601 taatttttta ttttctgtga agtcaaggtc ttgctacgtt gcccatgctg gtatcaaacc
    15661 cctgggctca atcaatcctt ccacctcagc ctccccaagt attggggtta caggcatgag
    15721 ctaccacact cagccctagc ctacttgaaa cgtgttcaga gcatttaagt taccctacag
    15781 ttgggcaaag tcatctaaca caaagccctt tttatagtaa taaaatgttg tatatctcat
    15841 gtgatttatt gaatattgtt actgaaagtg agaaacagca tggttgcatg aaaggaggca
    15901 cagtcgagcc aggcacagcc tgggcgcaga gcgagactca aaaaaagaaa aggccaggcg
    15961 cactggctca cgcctgtaat cccagcattt cgggaggctg aggcgggtgg atcacctgag
    16021 gtcaggagtt caagaccagc ctagccaaca tggtgaaacc ccgtctctac taaaatacaa
    16081 aaattaaccg ggcgtgatgg caggtgcctg taatcccagc tacttgggag gctgaggcag
    16141 gagaatcgct tgaaccagga ggcggaggtt gcagggagcc aagatggcgc cactgcactc
    16201 cagcctgggc gatagagtga gactccgtct cagaaaaaaa agaaaagaaa cgaggcacag
    16261 tcgcatgcac atgtagtccc agttacttga gaggctaagg caggaggatc tcttgagccc
    16321 aagagtttga gtccagcctg aacaacatag caagacatca tctctaaaat ttaaaaaagg
    16381 gccgggcaca gtggctcaca cctgtaatcc cagcactttg ggaggtggag gtgggtagat
    16441 cacctgacgt caggagttgg aaaccagcct ggctaacatg gtgaagcccc atctctacta
    16501 aaaacacaaa aattagccag gtgtggtagc acacgcctgt agtcccagct actcgggagg
    16561 ctgaggcaca agaatcactt gaaccccaga ggcggagatt gcaatcagcc aagattgcac
    16621 cattgcactc ccgcctgggc aacagagtga gaccccatct caaaataaat aaataaatat
    16681 ttttaaaagt cagctgtata ggtacttgaa gtgcagtttc tactaaatgc atgttgcttt
    16741 tgtaccgtca taaagtcaaa caattgtaac ttgaaccatc ttttaactca ggtactgtgt
    16801 atatacttac ttctccccct cctctgttgc tgcagatccg tgggcgtgag cgcttcgaga
    16861 tgttccgaga gctgaatgag gccttggaac tcaaggatgc ccaggctggg aaggagccag
    16921 gggggagcag ggctcactcc aggtgagtga cctcagcccc ttcctggccc tactcccctg
    16981 ccttcctagg ttggaaagcc ataggattcc attctcatcc tgccttcatg gtcaaaggca
    17041 gctgacccca tctcattggg tcccagccct gcacagacat ttttttagtc ttcctccggt
    17101 tgaatcctat aaccacattc ttgcctcagt gtatccacag aacatccaaa cccagggacg
    17161 agtgtggata cttctttgcc attctccgca actcccagcc cagagctgga gggtctcaag
    17221 gaggggccta ataattgtgt aatactgaat acagccagag tttcaggtca tatactcagc
    17281 cctgccatgc accggcaggt cctaggtgac ccccgtcaaa ctcagtttcc ttatatataa
    17341 aatggggtaa gggggccggg cgcagtggct cacgaatccc acactctggg aggccaaggc
    17401 gagtggatca cctgaggtcg ggagtttgag cccagcctga ccaacatgga gaaaccccat
    17461 ctctactaaa aatacaaaag tagccgggcg tggtgatgca tgcctgtaat cccagctacc
    17521 tactcgggag gctgaggcag gagaatcgct tgaacccggg aggcagaggt tgcggtgagc
    17581 tgagatctca ccattacact ccagcctggg caacaagagt gaaactccgt ctcaaaaaag
    17641 ataaataaag taaaatgggg taagggaaga ttacgagact aatacacact aatactctga
    17701 ggtgctcagt aaacatattt gcatggggtg tggccaccat cttgatttga attcccgttg
    17761 tcccagcctt aggcccttca aagcattggt cagggaaaag gggcacagac cctctcactc
    17821 atgtgatgtc atctctcctc cctgcttctg tctcctacag ccacctgaag tccaaaaagg
    17881 gtcagtctac ctcccgccat aaaaaactca tgttcaagac agaagggcct gactcagact
    17941 gacattctcc acttcttgtt ccccactgac agcctcccac ccccatctct ccctcccctg
    18001 ccattttggg ttttgggtct ttgaaccctt gcttgcaata ggtgtgcgtc agaagcaccc
    18061 aggacttcca tttgctttgt cccggggctc cactgaacaa gttggcctgc actggtgttt
    18121 tgttgtgggg aggaggatgg ggagtaggac ataccagctt agattttaag gtttttactg
    18181 tgagggatgt ttgggagatg taagaaatgt tcttgcagtt aagggttagt ttacaatcag
    18241 ccacattcta ggtaggggcc cacttcaccg tactaaccag ggaagctgtc cctcactgtt
    18301 gaattttctc taacttcaag gcccatatct gtgaaatgct ggcatttgca cctacctcac
    18361 agagtgcatt gtgagggtta atgaaataat gtacatctgg ccttgaaacc accttttatt
    18421 acatggggtc tagaacttga cccccttgag ggtgcttgtt ccctctccct gttggtcggt
    18481 gggttggtag tttctacagt tgggcagctg gttaggtaga gggagttgtc aagtctctgc
    18541 tggcccagcc aaaccctgtc tgacaacctc ttggtgaacc ttagtaccta aaaggaaatc
    18601 tcaccccatc ccacaccctg gaggatttca tctcttgtat atgatgatct ggatccacca
    18661 agacttgttt tatgctcagg gtcaatttct tttttctttt tttttttttt ttttcttttt
    18721 ctttgagact gggtctcgct ttgttgccca ggctggagtg gagtggcgtg atcttggctt
    18781 actgcagcct ttgcctcccc ggctcgagca gtcctgcctc agcctccgga gtagctggga
    18841 ccacaggttc atgccaccat ggccagccaa cttttgcatg ttttgtagag atggggtctc
    18901 acagtgttgc ccaggctggt ctcaaactcc tgggctcagg cgatccacct gtctcagcct
    18961 cccagagtgc tgggattaca attgtgagcc accacgtcca gctggaaggg tcaacatctt
    19021 ttacattctg caagcacatc tgcattttca ccccaccctt cccctccttc tcccttttta
    19081 tatcccattt ttatatcgat ctcttatttt acaataaaac tttgctgcca cctgtgtgtc
    19141 tgaggggtg
//

