Tag | Content |
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EnhancerAtlas ID | HS102-08862 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr16:11960470-11961980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr16:11961353-11961364 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr16:11961353-11961364 | CATGAGTCACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH16I011866 | chr16 | 11960558 | 11960748 | GH16I011867 | chr16 | 11961101 | 11961990 |
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Enhancer Sequence | ATACGAAAAT ATTTCTTGCA AGTAATGTGG GTGCACAAAG CCTTCAGAAA CAATTTGAAG 60 GAAAGATTGA CAGTAACAAG AATTTCACTT AAAAAAAAAA AAAAAAAGAC AGCATCTCAC 120 TATGTTGCCC AGGCTAGAGT GCAGTGGCAA TTCACACGTG TAACCATAAC CCACTGCAGC 180 CTCCAACTCC TAGGCTCAGG TGATCTTGCC AACTCAGGAG TAGCTGGGAC TACAGGTTTG 240 TGCCACTGCA TCTAGCAAAT TTCATTTTTT TTTTTTAAAG ACTGTTAACA GGCTGGAGTG 300 CAGTGGCACG ATCTCAGCTC ACTGCAACCT CTGCCTCCCG GGTTCAAGTG ATTCTCCTGC 360 CTCAGCCTCC CAAGTAGCTG GGATTACAGG CGCACGCCAC CACACTCAGC TAATTTTTGT 420 ATTTTTAGTA GAGATGGGGT TTCACTATAT TGGCCAGGAT GGTCTCGATC TCTTTTTTTT 480 TTTTTTTTTT TTTTGAGACG GAGTCTCACT CTGTCGCCCA GGCTGGAGTG CTGTGGCGCA 540 ATCTCGGCTC ACTGCAGGCT CCGCCTCCCA GGTTCACGCC ATTGTCCTGC CTCAGCCTCC 600 CAAGTAGCTG GGACTACAGG CCACGCCCGG CTAATTTTTT GTATTTTTAG TAGAGACGGG 660 GTTTCACCGT GTTAGCCAGG ATGGTCTCGA TCTCCTGACA CCGTGATCCA CCCACCTCGG 720 CCTCCCAAAA AGTGCTGGCA TTACAGGCAC ACGCCTCCAC GCCCAGCTAA TTTTTGTGTT 780 TTTTAGCAGA GACTGGGTTT CACCACGTTG GCCAGGCTGG TCTGGAACTC CTGACCTCAA 840 GTGATCTGCC CGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGT CACCGTGCCT 900 GGCCTGAACC CCTACTTTAA TAGCAAGCTT GGTCCCAAGT TTTAAGCTAT GATTGGTTTA 960 ATGCCAAATA CCTAGAGGCT GACTGCCAAA ACCTCAAAGC GATTCACCTA AAGACAGTTC 1020 AAACAGGAAC TTAGTACACA GGAATGAACT GCTGTCATTC AAGTAGCCAC TGTGTATGTT 1080 ACCTTTATCA TTAACTTCTT CTTGCCCTTG CACATTGAAT GAAAAGGGCA AGCACTATTT 1140 GGTCTCTTGA TCTTTATTAA AAATCCTGAA TGTAGAGGTT CATAGTTCTA ATAATAATTG 1200 ACGTTTCCCC CAACTCTACT GTTCACATAA AACCACATAA CTGTGATCTA GTTATTTATT 1260 ATTCAGCATC CCTAACTTCC TATAGGGTTC TTATTTTTGT TTCCTAAGGT TGTCGTATAC 1320 ATTATACAAA AGACTTGCAT GCCATATGCA AGCAGATGAC GTTTGTGAAT CCCTTATGTG 1380 ACAGAGCTTA TTAGATCCAT CCAACAAACC TTTTGGTAGA TGGTTCCAGT ACCTGATACA 1440 AAAATAAAAG GATTGTACAA AAAAGGGCAT GGTTTTTGCT TGTTACAACA CAGGTAATTA 1500 CAAACGACAA 1510
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