Tag | Content |
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EnhancerAtlas ID | HS091-14027 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:95677220-95679550 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chr14:95677529-95677539 | ATGGAATGTG | - | 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: 1 | ID | Chromosome | Start | End |
GH14I095212 | chr14 | 95678392 | 95679788 |
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Enhancer Sequence | AGGAAAAACA GCAGCGGCGG CCAGGATGCT GGTTAGTAAA CAGACTCAAA GGTGCAAGGT 60 CAGCATGCAG CAGCCGCGTG AGTTTTTGAG TGGGGCAGAG CTGCCGACCT CGCCAGGTGA 120 AGACGCCTTC ATCCCTGAGC ATGGGAGAGC TGCCCTGAAC CACTCACATT TCCATTTCCA 180 GCCAAATGGA ATAGGAGGGT ATACACTGAA CAAAGAGGCA AAATAGGACC CTGGGTTCCC 240 CAATTCCCAG ACACATAAAG GACCAACTGT ATAGACCATT CCTTGTATCA GTGACATTGA 300 AAACATAACA TGGAATGTGC TGTGCCATAA AAATGGAACC AGAAAGACAC AAGTTTGTAC 360 CTCAGCTGTC CCCTCTATGC TTCTAGTGCC ATGGCCTTGG GCAAGTCACC TACCTCTCTG 420 AGCCTCAAAC TCCACACAGT GAACTTGCTG GGGCTTTTGT GGGGAAAGTC GAGCCTGGCC 480 CCAGAAGAAC GGCCAAGTCA TAGGGTCAAC CTAATATACA ACGTTGGGAG CCCAAGAAAG 540 CCACTCACTA ATGACAGCTA CTATTATCAG TAATAGAAAT AAAAGCACCA TTGTAAAAGT 600 GAGGGGCAGA GAGCTTTCAC TCTATTTTGT AGAATGGAGG CTACCTCAAC TTTTTAAAAG 660 TAAAAGTGAA GGACAAAAGA GGAGAGAATC TTGCCAGGCA CTAATTTCCT GTAGAATCTA 720 TCCTGAGACT CCACCAATCT CTCAACCGTG GTCAATAAAC GCTCTTAAAA AAAAAAAAAA 780 AAACCAAAAA CAACCAAGTA CCTTTTTATT TGGAAATCAT TTAAGACCCA AAAGAAGTTG 840 AAACACAGTA CAGAGAGTCT CTACTCTTTC CCCAGCTTCC TCCAGTGACA GCATCTTATG 900 CTACCAGGGT GCGTTATCCA AACCAGAACA CCAATACTGG TCCAAGACAA TTATTAATCA 960 AGCTATAGAC TGCATTTGAA TTTCACATTT TCACAGGTGT TACTTTTCAT GGCGGTGGTG 1020 TACAGATTAA TGTAACCACC ACAATAGAGA AACAGAACTG TCCTATCACC CCAAGACACT 1080 TCCTCTCCCA TACATCACAC CCCCCTTCTA CCCTAACCCC TGACAATGAA CTTTTTTTTG 1140 GTTGATATTT ATGTAAACAA CATTTAATGG TGGTTCACAT TTGTCAATTT CAATCTACCA 1200 CGCTTGATCT CTCAATCAAA ACTCTGAAGA TCCAACCTCT CTTCCCTCTT TTATTTCCAC 1260 ACACAGGGGA TAAAGGAATC AATATTTGTG AAGTGCTTAA TATGGGCTGG CACTGTGCAA 1320 GGTGCTCTTT CATGGATTTT ATTTAATTTC ACCTAATTGT CCTGGAAGGC AGTGTGTGAT 1380 AGGATACTAT TTGCAGTTGG GGCTTGGAAA GGTAAATGAT TCACCAGGAT CTCAACCAGT 1440 CTGTACGCTG AGGAGCTGGG GCGGCCCCGA GTTGGTTTGG TTTCCACCAC ACTGGTCTGG 1500 CATTTGTGCC CATGGTCCAG GGGCTGTGGG CCTGCTGCTG GTAAAAAGGC CTGATACAAA 1560 ACTGCTAAAA TCACTCTGCT GCCGGTGTGG GGTGAAACAG GGCCGGAACT TGGCTCCAGT 1620 TCCCGTCTCG ATTTTGGAAG GTCCGACCTA ACTTTGAGTA TGTTACAGCC TTTATTATTA 1680 CTATTTTTAA AGTAGGTACA GACTCTGGAA GATACCCTGA AGCTTAAATG CACACAAGTC 1740 ATTAGAATCC AAGAGACATG CCCATGTTGA GAGGCAACAT GATGAAGGCT CCTCTGATCT 1800 GTATTCAAAT CTTATCAGCT TTGTGCAAAC CAAACATTCT GCAAACTGCA TTTTGTGTGT 1860 ACTGCAAAAC CAGAAAAATG CAGGGTTTCC TGTTCTGACA TTCTTTTTTT TTTTTTTTTT 1920 GAGATGTTGT CTCGCTCTGT TGCCCAGGCT GGAATGCAGT GGAGTGAACT CGGCTCACTG 1980 CAAGCTCCGC CTCCCAGGTT CACGCCATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC 2040 TACAGGTGCC CGCCACCACG CCCGGCTAAT TTTGTTTGTA TTGTTTAGTA GAGACAGGGT 2100 TTCACCGTGT TAGCCAGGAT GGTCTTGATC CCTGACCTGG TGATCCACTC GCCTCGGCCT 2160 CCCAAAGTGC TGGGATTACA GGCATGAGCC ACCGCGCCTG CCCCCTGTTC TGATATTCTA 2220 TATGAAGCAA TGGGCACATA CATAACTGGC ACCTTAATAA ATACTAATTC TCCTTTCCTC 2280 TGCCTGAAAG CAGCTAGTTA AATGAAGTAG TGTGGGGAGA GGGGCTGCGG 2330
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