Tag | Content |
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EnhancerAtlas ID | HS043-01348 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr1:52669510-52670650 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr1:52669658-52669669 | ATATTAATTAT | + | 6.02 | NKX2-5 | MA0063.2 | chr1:52670175-52670185 | ACCACTTGAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:52670182-52670197 | GAGGTCAGGAGTTCA | + | 6.22 | REL | MA0101.1 | chr1:52670483-52670493 | GGGGATTTCC | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCTAAATA AGCCTATCAA AGGCATTCTT CATTTCTGTT ATCGTGTTTT TGATCTCTAG 60 CATTTCTTTT TGGTTCTTTC TTAGAATTTT TCTATACTTT CATTGCCCAT CTGTTCTTGC 120 ACGCTGTCTA CCCGTTATAG CCCTTAGCAT ATTAATTATA GTTGTTTTAA ATTCCTGGTC 180 TGATAATTCT AGCATCTCTG CTATATCTGA ATCTAGTTCT GATGTTTGCT CTTTCTCCTC 240 AAACTTTTTT TTTTTTTTAA CCTTATGCCT TGTAATCTTT TCTTGATAGC TGGACATGAT 300 ATATTGAGTA AGAGGAACTG CTGAAAATAG GCCTTTAGTA ATGTGATAAG CTGTTGGGGG 360 AAGGGGAGCA TTCTATAGTT CTACGATTAA GTCTCAGTCT TTTAGCAAGC CTCTGCCCCT 420 GGACTGTGAA CTTCACAAGT GCTTCTCAGT TTTCTCCCCT GTTTAGAGGG GACAGGATAG 480 CAAGAATGGG CTGGAGCTGG GTGTTTCCTT TCCCCAGGTC AGTTAGGCTC TGATATAACC 540 CCAGCAGGTT AGGCTTTCGT CAAATAGTTT CTGCTGAGGG CAGACCGTAT TAAGAATAGA 600 ATGCTCTTAG GCTGGGGTGG CACATGCCTG CTAATCCCAG CACTTTGGGA GGCTGAGGTG 660 GGCAGACCAC TTGAGGTCAG GAGTTCAAGA CCAGCCTGGC CAAAATGGTG AAACCCCGTC 720 TCTGCTAAAA ATACAAAAAT TAGCTGGGCA TGGTTGCGTG TGCCTGTAAT CCCAGCTACT 780 CAAGAGGCTG AGGTGGGAGG ATCACTTGAA CCCAGGAGGT GAAGGTTGCA GTGAGCTGAG 840 ATCTCGCCAC TGCACTCCAG CCTGGACAAC AGAGCGAGAC CCTGTCTCAA AAAAAAAAGA 900 AAAGAAAAAA GAGTAGAATG CTCTGGCTTA TTTCAAAATG GTTCCCTTTC CCCTTTCCCT 960 GCCAGAAGAA TGAGGGGATT TCCCCCTTGA TGCTGTGAGA TCTAGGTCAA GCTTCCCACG 1020 AAAGTGTGGG AGTCCCCTTG AAGTTTTTAA CTCGCAGAGT TGTCCACACT AAGCCTCTAG 1080 CAATTTGTCA ATTATAATTC AAGCTTTTCT GCCCGACATC TGGTTCCCAC AGAGGTTCCT 1140
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