Tag | Content |
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EnhancerAtlas ID | HS091-24062 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:40162220-40163670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:40162806-40162825 | AACCGCCACCTGGTGGAAA | - | 6.72 | EWSR1-FLI1 | MA0149.1 | chr19:40162371-40162389 | GTTTTCTTCCTTCCTTCT | - | 6.18 | EWSR1-FLI1 | MA0149.1 | chr19:40162379-40162397 | CCTTCCTTCTTTCTTGCC | - | 6.57 | EWSR1-FLI1 | MA0149.1 | chr19:40162375-40162393 | TCTTCCTTCCTTCTTTCT | - | 6.96 |
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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 |
GH19I039672 | chr19 | 40162741 | 40162870 |
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Enhancer Sequence | TGAGCAAACT ATCGCAGGGA CAGAAAACCA AACACCGCAT GTTCTCACTC GTAGGTGGGA 60 ATTGAACAAT GAGAACACTT GGACACAGGG TGGGGAGCAT GGGGGGTTTT TTGTTCGAAT 120 CCCCCTCTCT CTGTCTCTGT ACGGGGGAGC TGTTTTCTTC CTTCCTTCTT TCTTGCCTAT 180 GAAACTTTTC ACCCCTTAAA ACCACTCCAC ATGTGTCCAT GTTGTTAATC TTATCAGCAC 240 GAGACCAAGG ACCCTGGTTC CCTCCAGTCA TCGGAGCCAT ATCTTTTAGG TGCATTGGCC 300 AGGAATGGGA ATTCATTCAT CAGACTGGTG AGTATGGAGC AAATCTCAAC TTTAAATCTG 360 TCTTTTAATC TCTAGGCTCT CTTCCAGCTA TCCTGCCACC AAACTTTCTT TCTCTCTCTA 420 CCCGCGGTCT CTTACTGTCT CTCTCACTGT GTCTAATGTG CAGGAATCTT TACAGTTCAG 480 GGAAACAGGT CTGTTAGAGA AGATCATGAA TCAAGGCAGG CAGTAACTCA ATAAACGTCT 540 GTCTCTCTAA GGTTTCGCTG GTGAGCACAT GGTATTTCTA AGCCAAAACC GCCACCTGGT 600 GGAAATAAAA ATCCTCTTCA TGAGACACTT GGTTCTCTGT GGTACGTTGC AGCTTCACAA 660 TTTCTCCATT TTGCACTTTT TTACTGCTAC TTCTGTGGAC GGGAAACTCT GGTTTCAACC 720 ATTAGGAGTA AGATGTCTTC CACAGCCAGA TTTTAGTCCC AATATTGTCC CATCAGTAGG 780 AAAACTGCCA TTCGGTTCCT ACACTCTTTT AAGGCACCTA TTCTGTCTCC AATTAAGACA 840 GTACTTAATT GGTAAGGGGA TATTAAGTTT AGAAGTTAAC CAGAACAGTT TTTTTTAAAG 900 GGTAAATGCA TTAGCACGGG TCATAATAGC AGGCAATCTA GCACATTGCC TCCATTAAAG 960 GAGCCTTGCC CAGAGGTGAC ACAGTCTCCC CGGAGATCCG TTTTCAGGGA GCCAGGCAAA 1020 CTGCACATGT TTAGGAAATC AAAGGTAAAT CACACAAGGC AGATAAGCTA AGACTGCATG 1080 GGTAAGCACG GGTAGCCCCA TCACTTAGTT CATCCAGCTC TATGGCTTGG AGGACCACAC 1140 CTACAGCCAT GGGTGGCACA TTTAACATGG TGCCGGGATC CAGAAACCAG GGAGGGGAAG 1200 TAATCAGAGG ATGCTCCCTG TCTGCTCCTC CACTCTGGGT CATACCAAAA GGAAGGAGAC 1260 TAAGAAGATG CTTTGTATTC TTTCTTCTTT TTCTAAATGG ATAATAAATT ATCTTTAGGT 1320 TGCACCCCTC TGGAGTGCAC TCTGAAACAC TGAAACTTCC TTAATCTCAA AACTGTAAAG 1380 AGAAAAGCAA TTTATTTTCT TTTGCACAAG GACATGGCAT TTTTACTAAA TGGGAGGGAA 1440 GCGGTTCTCA 1450
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