Tag | Content |
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EnhancerAtlas ID | HS091-13780 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:78328320-78329250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr14:78328718-78328737 | TGGCCAGCAGATGGCGCCT | + | 7.41 | EWSR1-FLI1 | MA0149.1 | chr14:78329032-78329050 | TTTTCCTTCATTCCTTCT | - | 6.33 |
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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 |
GH14I077862 | chr14 | 78328641 | 78328770 |
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Enhancer Sequence | GGCAGGGAGT GCGCTGGGGC CACATTGCTA AGGGAGGGCT GGTGACAAGC AATGGGATGA 60 GACCTCATGT CCTCTAATTC CCAGGCTGGT GATTCGTCCC CTACATAACA GCTTCTGTTT 120 GGCAGGAAAA AAAGCAGTTG TGTGTGTGTC TGTGTGTATC TTGGAAGTTT CTCAGCTAGT 180 ATTACCAGAA AGAAACTTAC TTTTTTTCCT TTATTTGGTT GTTAGGCTTA TATCCTGAAA 240 GACAGGTTCC AGGAAGCAAT CAGGAGCCCA GCCTCTGGGA GGTGGGGTCG TTTCTGCCTC 300 CTCAAAAGTG ACCTCGTTCT GGACTGGGTC AGGGGTGGTC CCAGCCTTGG TCCCCTTGAC 360 TGCCCTTGGG GCTGTGGGTC CAGATGCAGT GCTGACCTTG GCCAGCAGAT GGCGCCTGAG 420 CTTGCAAGTC AGGGATGGTT GTAAAGACCT GGCCCTTCTC TTTGTGGGGG GATCCCTGAC 480 CAGGTGGATG AGACTGGGGG TCTTTCTGCT CTTGGGCATG GTTCGTGCTG TTGAAGGAAC 540 GCAGGCTGAC ATCTCTACAC CCTGAATGGG CATGCATAGC CTCAGCCACG AGGCTGTTGA 600 CCACCCTGGG TGCCTCAGCC CTTGACTCCA TGTTGGAGGA CGTGGTATTG GAGTTAGGAG 660 TTCTCTGATG CTCCGCAGTC TCTGATGGCC AGTGATTCTG TGCTTCAGCA CCTTTTCCTT 720 CATTCCTTCT CTCTCCTGCT GGTCTACGCG GTTGGCATTT AGTGAAAAAG GACAGTGCCG 780 GACATTTGGG TGTAGCCAGG GATGGGTACG ACCTCATTCC AGTCCTCACA GTCCAGGGTC 840 ATGGGAGGTT CACTCATCAT GGTAATACAT GGCCACATAG TGCCCAACGA GCTTGCAGAG 900 GAGAGAGAGG TTGCCTTGGG CAGATGGAGG 930
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