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EnhancerAtlas ID | HS012-18446 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr3:130421700-130422360 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr3:130422013-130422024 | TCAAGGTCAAA | + | 6.14 | Hnf4a | MA0114.3 | chr3:130422015-130422031 | AAGGTCAAAGTCCTTT | + | 6.49 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGTACACTA TTTGTTTTCC TTACACAGTT AGCCATTCTA TAATTTTTTT ACTTTTTTCA 60 TGATCATATT CCATCTAATC CATTCATTCA GCAAATCTTG TTATATCCAG GATCTGATCA 120 TTTCCCACCA CCTCATACTG CTACCAAGCG ACCAGCTCTT GCCTGATTAT TTAATAGTCT 180 TCTAACTGCT TCTGCCCTGC TCCTCTTCAG TCTATTCTCA ACATAACAGC CAGAGTAATT 240 CTGTTGACAA CTAACTCAGA TGACATCTCT CCTCTACTCG GAACTCTTCA AAGGCTCCCC 300 ACCTCACTCA GAGTCAAGGT CAAAGTCCTT TACAACAGCC TACAAAGCCA TATCTAACTG 360 GCCCCTCTTA CTCCTCCACC TCGCTCACTT TGCTCCAGCC ACAAAGACCT TTCTGCTGTT 420 CCTCAACCAT GCCAAACATG TTTCTTCCTC AGGGCCTTTG AAATGCCTGT TTCCTCTGCC 480 TGGAATGTTT TTCCACAAGA TATCCATATG GCTTTCTCTC ACTTTTTTCA AGTCCTTCCT 540 CAAATGTCAT TTTCCCTGTG AGGCATTCTC TGGTTAATTT ATTTAAAATT CTACCCTACC 600 CCACCTCTAC TGCATTTCCT AGCTTCCTTT CCTGCTGTAT TTTTTACCAC AATTTTTTTT 660
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