Tag | Content |
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EnhancerAtlas ID | HS091-17021 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr16:30438600-30440370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX2 | MA0688.1 | chr16:30440172-30440183 | TTTCACACCTC | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATTACAGGT GTGAGCCACC CCGCCCAGCC CCTTTTTTGT TTTTTTTTTT TAAGGCAGAG 60 TCTTGCTCTG TCGCCCAGGC TGGAGTGCCA TGGTGTGATC TTGGCTAACT GCAGTCTCTG 120 CCTCCTGGGT TCAAGCGATT CTTGTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGCGC 180 CCGCCACCAT GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTC ACCATGTTGG 240 CCAGACTGGG TCATCACCTT GTGTTCTTTT CCTCATAGAA CTTGTCATAA TTCCAGATCT 300 TCTAATATGA GATTACTGAT TTACTGTCAA TCTCCTTCCA CTGTGAAGGT GGAAACCTTT 360 CTGCCTTGTT CCAGGCCATA TCTCAATTCT AGAAGACCTA GCACATAGGT GATGTTCATA 420 AATCTGTCAT GAGGCCATGT GCAGTGGTTC AACCTGTAAC CCCAGTGCTG CGGGATGGTG 480 AGGCAAGTGA ATCACTTGAG ACCAGGAGTT TGAGACCAGC CTGGGCAACA ACAGCGAGAG 540 ATCCCATCTC TACAAAAAGT AAAAATAAAT TAGCCAGGCT TGGTGGTGGC GCACGCCTGT 600 AGACCCAGCT ACTCCGAAGG CTGAGGTGGG AGGATCGTTT GAGCTCCTGA GGCTTCAGTG 660 AGCTATGATC ACACCAGTAC ACTCCAGCCT CAGCAACAGA GTGAGACCTT TTCTCTTAAA 720 AAAATGACTG TCCTGGTCTA GGGCTCATCG CCTCTTGCCT GGTCTACACC AGCCAACTCT 780 CTGGTGTCCC CTGCCCCATT CTCTCAGTGA TCCATCCAAT CCACCCTGTA GACACAGTGA 840 CCTTTCCAAC ACTCATATCT GGTCAGGTCT TCTGTCCAAA CTCTCCATCA TACTCTAGCC 900 CTAATCATAT CTTTGTGGGT TCAACTCCCA CCCCTCTCCT CCACAGCCCT ATCACTCATC 960 CAACGTGTGC CTATTGAGCG CCTACTATGC GCTGGGCACT TGGGACACAT CAGAGAAAAC 1020 AGATCCCAAA TCCCTGATTT TTCCTGAGAT GCTTACAATG AAGGAGCGTC AGATTCTCCC 1080 TGAATTGAAC TTGCCCTTTC TTGCCTCACT GCCCCTGCAA ATGTAGTTCC CATGTCTGGA 1140 ATGCCACAGG CAGGTCCTCT ACAGAATACC TTCCTTTCAG CCCCAGAGGC AGAGGAAAAG 1200 GGTTGTTGGG CCAGGCGTGG TGGCTCACCC CTGTAATCCC AGCACTTTGG GAGGCCAAGG 1260 CGGGTGGATC ACCTGAGGTC AGGAATTTGA GACTAGCCTG ACCAATATGG TGAAACCCCG 1320 TCTCCACTAA AAATACAAAA ATTAGCCAGG CGTGGTGGGG GGCACCTGTA GTCCCAGCTA 1380 CTCGGGGGGC TGAGACAGAA CTGCTTAAAC CCAGGAGGCG GATGTTGCAG TGAGCCGAAA 1440 TTGAGCCACT GCACTCCAGC CTGGGCGACA GAGCGAGACC CCGTCTCAAA AAAAAGCCAA 1500 AAAAACAAAA AACAAAAGAA GGGAAAAGGG TTGTTGCCAC TGCTTCTTCC TAGACGGGAC 1560 CTGTCCTGAT GCTTTCACAC CTCACACCTC TCTCTTCCAG GAGGCTGAGT GCCCCTAGAG 1620 GGCAGGGACC CGTGAGTCCT CTCTGCATCC CAACAACAGC AAAGAGCCTA GCAATCAGGA 1680 GGGGAAACTG AACCCATGAA TGTTTGAAGA CCAAATAAAT GCTCCCCTCC CCTCCCCCAC 1740 AACTCAGACT CTACCAGGAA GCTTTCCATC 1770
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