Tag | Content |
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EnhancerAtlas ID | HS091-34453 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:58517540-58519170 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:58518650-58518669 | GGCCGCCACCTGGTGGCCA | - | 8.59 |
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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 |
GH03I058532 | chr3 | 58518328 | 58518928 |
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Enhancer Sequence | TGAGGGCAGA GAGAGTAGCG GCCCGTCACA GGAAGACCTG TGCATTGCTT TTCCCAACCA 60 ACCCAGCCTC CTGGGGCTGG GGTTTTGGAT GGGTACCTCT GGGGCCCTGA AAAGTCACTG 120 ATCAAAGAGA GAGGGGATTG CCCCCAAAGA ACCAAGCAAA CCTAGCAGCG TTGGCAAAGG 180 CACTGTGAAA TGATCCAGCT TTTTTTTTGC CCCCCCCAAC TATTAATGAA TTACTCTGTC 240 ATCAACCTTA TAATAATGAA TACAGATAAT TATCATTTAT CAAAATCTAG GTGGCGCTAG 300 ACCCTGTGAT AGATGCTTTC CAGTTCTTGC AGGGGAGAGA GGATGATGAG TCCCATTTTC 360 CAGTTAAGGA AACAGGCTCA GAGAGTAGAG TGACACACTG AAGGTCATTG GCCTGGAGGG 420 GCAGAGCTAG GATTCATCTG TACCCTGGTC TGTCTGATCT AAAAGGCTGG TTTCTTTTGT 480 CTTCATTTTT GACAGTGGTC ATTTATTTTC TCTCTCTCTT TCTGTCATCA CTCTCTCATC 540 TCTCTCTCTC TTTTTTTTTC TTTTTCTTCT TTCTTTCTTT CTTTTGTTTT TGAGACAGAG 600 TCTCACTCTT TCGCCAGGCT GGAGTGCAAT GGCCTGAGCT CGGCTCATTG CAGCCTCTGC 660 CTCCCAGGTT CAAGCAATTC TCCTGTCTCA GCCTCCCGAG TAGGTGGGAC TACAGATGCC 720 CGCCACCACA CACGACTAAT TTTTGTATTT TTAGTAGAGA TGAGGTTTAA TGATATTGGT 780 CAGGCTGGTT CAAACTCCTG ACCTCAGGTG ATCCACTCAC CTCGGCATCC CAAAGTGCTG 840 GGATTATAGG CATGAGCCAC CGCACCCGGC TCATGTCTCT CTCTTATGTC TCTGGTCTCT 900 GCCTGTGTCT CCCTCTCTCT ATGTGTCTCT CATCTCTGTC ACTCTCCTGC TTTAGTTGGG 960 CTCAGCATAT TTGTTTTAAT TTTTTCCACA CAAGGTGTGG GTCCCCAAGT GCCACAGATG 1020 TGTCCTTGGA GGTGAAATTC TCAAGTTTGA GGAAGGGGAA ATCCCTCGTT GGGGCTTGGT 1080 AAATCACCAA GCCTCAGGGA CGCTTGATGT GGCCGCCACC TGGTGGCCAC AGCAGGAGGT 1140 ACGGCGTTGG TGGCCTGATG GGGGCTGGTG ATGGGCGTGA GCCTTCCTGG GTGTCTGCAG 1200 CAGGGGCAGG CAGGCGTATT CTTTCCACTG TGTCATCACA GGGCCTGTGC TCTGGCTGGT 1260 GGCAAGCTCT GCCACTAACT CGGGAGATGA GAGGAACCGG GGTTGTGAGG AGTGCCTAGG 1320 ACTAGACCAA GTGTGTGTGT TTGTGCGTGT GTGTGTGAGT GAGGCCTTGT CTCTCATGGA 1380 TCGATTGTCT CCTCTACTTC AAAGTTCCTT TGGGGACTTT CCAGCCACTC ACTAATGAAA 1440 TGTTTAATAT CCCACCTATT TTACAGAGTA AGAACCTGAG GCTCAGGTTG GTGAACTGAC 1500 TTGCCCAAGG TCAGCAGCCT AGAACAGAAA ATCAATCTGA GGTCTGTTGG ACCTCAAAGC 1560 CAGTGCTACT CTGCCCTCCA ACATTCTTCT ACTTGGGGAG AGTTAAGGAA GGGGGGTGGA 1620 TGTATACTCA 1630
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