Tag | Content |
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EnhancerAtlas ID | HS026-32334 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr8:21745770-21746910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr8:21745912-21745926 | AAGAGAAGATAAGA | + | 6.13 | Mecom | MA0029.1 | chr8:21745917-21745931 | AAGATAAGACAACA | + | 6.59 | PLAG1 | MA0163.1 | chr8:21746222-21746236 | CCCCCTCGGGCCCC | - | 6.65 | Znf423 | MA0116.1 | chr8:21746250-21746265 | GACCCCTTGGGTGGC | - | 6.6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAAAAGGAAA GCAAATCTGA TAAACTAGCC TCCACTGAGC TTGCAGTTAG AGAACTCAGT 60 GACAGCCCCA TCATTGTCAC TAACGTGATG AGTGACTTTG GGCAAATCCC TTAGTCTCTC 120 TAGACTTCAG TTTCCTCTCT ACAAGAGAAG ATAAGACAAC AGGGTATCTT TTTGCTCAGA 180 ATTCTATGCT TCTGGGATGT TAGCAATTTA ATGTGTTCCC CTCTTAGGGA CTCACATTAC 240 ACTTTAAAAA AGACTTTAGT AAAAAGATGA ATAAATTCAG AGGAATGAGC CCCCAAAAGT 300 GAAATTCCAG GTTTAGTGGC ATGTGGGGGA GAGAGATTTT TTAGGATGGT TGGGTGAGGC 360 AGTTGTAAAA TCACACAGTC AGCAACCAGT AACTGCTGCC TCTGCATGAG GCCGGCTTCA 420 CCTCCAGATG GTAGGCCTAC CGCTGTCTCA GACCCCCTCG GGCCCCACGA GGCCTGCCCT 480 GACCCCTTGG GTGGCCTTCC ATTCCATCAG GAATCAGGAA ATCATATCTC TGATAGGGAT 540 AAATACTGCA TTTTTAATTT TTGAAAAGCA AAATATAGGT ATTTATTTAC ATTCATGTCC 600 GTGTATACAC ACACACACAC ACACACACAC ACACACACAC ACACAAACAC AGTTGGCGAC 660 AGGAAAGGGC CAAGAAGAAA AATCAGCTTT GACAACCTAA TAAATGTCAA TTTCTGAAGG 720 GGGCTGAGTT AGAAGATGAA TCCTCAGAAC TTTAATTGGA GACATGATGC TCTCACTTTG 780 CCAGCACCCC CACCTCTCCC GATCCCTCCA CAGATAGCAA AGCCCTTGCC TTCCTCTAAT 840 TGACAAGAGG CCTCTGTCTG CTAGGATTTG CCTCTGGGAT GTCAAGAGGC CCAGGGATGG 900 GGTGAAGGTG GTGCTCTAAT GCCCTTCAGA GAGAAGAGGT GAAATAGCAG GATTTGTGTC 960 CCAAAGGCAG ACAGCCCAAT GGGCTGAGCA GTCACAGATT TGCCCTACGC TGTGCCTGCC 1020 CTACGTGAGA CCCTGCAGAG ACAAAGGGGT CCCCCCTGAC TAGTGATGCT TGCTTTCCAC 1080 CTAACAGCAA GTCAGGAGGC TCCCTTTGGA TCCCCGGTGG TACCCTAATC CAGGCACAGT 1140
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