Tag | Content |
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EnhancerAtlas ID | HS091-27268 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr2:112878880-112880480 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:112879428-112879447 | TATCCAGCAGGTGGTGCCA | + | 6.31 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 112879197 | 112879260 | chr2 | 112879312 | 112879561 |
| Enhancer Sequence | TTCATAGATT AGAAAACTGA GAGAGAGGTT AAATAATTTG ATAGTTTACC ATCCTGGCAG 60 GTGGCAAGGC TGGTATAATA CTGGTGGGAA TCATCCTAGA AGGGTTGTCC TCGAAGTCCT 120 GAGGAGAGAG GAGTTTCGGT TAACAAAGTG CTGTTTGCTT GTTAGAGAAG GTTAAGTAAG 180 ACAATGTATC TAAAGTGCCT GGTGCATAGC CTTCAGGAGG CAGCTAAGGT TAATGTGAAA 240 GGTACAGCAA TGATTGAGGG GTGACTGAGA CTCAATTGAA ACAAATGGCA TATGAAATTC 300 AAACACATTC CAGGATTGAT TCACTTGTAT TAAGATGAAG TTACCCAGAG CAAGTTTTAT 360 GCCCCTTAAG TGATAGGGAA TGTACAGCTA CATTAACAGA GGTGACCTGA TATTTACATC 420 TGGTCAGAGG CTGACCTGAT TTATATCTGA TTTCAGATGT AAATAATTTT GACAGTATTT 480 CCTTAAAATC ATTTTGAAAA AACAAGAAGC TGCAATGGAA GTTTATGCAC AGGAAAAAAT 540 GTGAAAGCTA TCCAGCAGGT GGTGCCAAAG TAATGTCTCT TGAAGAGTTC TAATCTTTTT 600 TTCTTTTCTC TAATTCTTCC CTTTACAGAT TTTATAAATT TACTTACCAA ATGCCACTAA 660 ACAAATTTGG GGATGAAGAA AAAAACTTAA AAATAATTCA CACAGCACTG CCCTGGAAAA 720 ACAGTTATTT TGGTATATTT TAAAACTTTA AAGCTGGAAA GAGCCTCTAA GATCATCTTA 780 CAAATGAGGA AATGGAGGAC CAGGAAAGTG TCACTGGCTA CAGTTCCCTC AGACCAGGGT 840 TGAAGACTGC CTCCTAGTTT GTTTTTCTCA CCTCTGGTCC TTATTGTCAG GGGGAAAGAG 900 ATGCCACAGA AGGGTTGGAC TGGGCATCAA AACTTGAAAT ACATTTTATA TACTTTGGTG 960 ACCACTTGCT ACGTCATTTC ATATGACTTC ATTGTCTTTT CAGCTTCCAA ATTCTTGTTT 1020 CTACATGGTC ATAATTCCAG TTCTCTGTTT CTTCATTTGA TAAGTGGAGA TTTTCTTGGG 1080 GTTCAGTGGA GTCTGCTGGA AAGGCTTGTC TTTATTTGAC CTGAGTCACA GCTTTCCCAG 1140 TGCTAAATGC CTCTTTCCAG GGGATACTTA TTAAAAATAT TCACAGGCAT GTTTTTTAAT 1200 GTCACAGCTG CCTAAAGCAA AAAATAACAT TCAAAGCAAA CAACAGACTG ACCAAAAACC 1260 TTAAAAGGAA AGTCTAAAGA ATGAGATGAC CATAAGGCCT TTGAAAAACC TTCAACATAC 1320 TTACAGGAAT CTAAAAGGTC ACATGCATGC ATAGGGCTCT GCATGCTCAG CAAAGACCAC 1380 AAACAAGAAG TGAAGGCTAA GGCAGAGTTA GTTGTAAACT GCCTGAATGA GTGCTGAAGG 1440 TGTGCCCCAC CATACACACA AGCACCTCGG CAAAGACTGG GAGATTTACT GGTTCCGAGA 1500 GGTTAAGAAA GTCTCTGTCC AATAATTGTC TAACCATTAC ATAACTGAGT AGAGACTTCA 1560 GTGACCACAT ATCACAAAAT ATACAGACTT TACGGAATTA 1600
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