Tag | Content |
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EnhancerAtlas ID | HS176-43579 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chrX:69699120-69700130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chrX:69699796-69699812 | CAGGTCAAAGTACAAA | + | 6.13 | NFIA | MA0670.1 | chrX:69699916-69699926 | GGTGCCAAGT | + | 6.02 | ZNF263 | MA0528.1 | chrX:69699674-69699695 | GGAAGAGGGAGGGGGTGGAGG | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCCCTTCAG AGCACTAGCC CTTGTGCTGG ACGAGGAGAG CTCCATGCCA ACCCAGCCCT 60 TCTTATTTAA CTAGTGGGCT AGGGAGTATG TACTCCCAGT TCTAAAATAA CGCTTCTCAC 120 TGTATGCTTA GGTTGTGTAT TTTATGGTCA GTGTCTCCTC CCTTTTGTGA GCTGGCTTCT 180 TCCTTTTAGC TCATGAATGA CTCAGTATGG GAAAATTTCA GTTTGCTCTA ATTGTAAAAG 240 ACTGTTGGGT GATTGTTGCT AGTCAGCATT CAAATATCAG TCAAATGTTC AAAGTACTTT 300 GCTTGCAATC TGTGCTTTGA GGGGAAACTT GCCACCCCCC CATCCCCTTC CATGTATGCA 360 TAATAGACAT CAGGATTTGT ATCTGAGCAT AGCAACTATC GCAGTGTTCT GGTACAGGAT 420 CTCTTTTAAG AGACCAAAGA ACTGACAGGT TGCTGCATTC TGGATGTTTT ATTGTGATTC 480 CATTCCCCCC TCACCACCCG CTGCACTGGT CTGCTGTATC TATGAATCAT GGGATGTATA 540 GTGTATGTGC CCTAGGAAGA GGGAGGGGGT GGAGGGAACA GATAGGTAGC ATGGAGTATA 600 TTGCTGCTGA AAGCTATTCC AAGATATTTC CAAGGTTGAG CTTCTCTGAC CCTTGAGGCA 660 TAGCTTAATA CTTTGTCAGG TCAAAGTACA AATCTCCTGG GGAGTTGGAG TGCCAAGTGA 720 ATACTGTGGA CTCCTCATAG AATTAGGGAT AGCTTCCTTC TTCCTGCTTT GGCTTCTTGG 780 CAAAACTCCA AAATCTGGTG CCAAGTACAT TGTATCCTCC AAGGTTAAAG CCCTTAGAGA 840 AAGGTGGTGG GGATTACTCT CCTGAGCCAG AAGTTGCTAC AGTATTGTGT TTAATGCTTA 900 GGTGTGGGGT CATATCAAAC TCTTGGGCTG AACTTTTTCT AGTGGCCTCT GATACCTGGC 960 TGGGAAGTTG CACTTGCTAG TTGCTTGGCA ACGTGACAAC TGCTCTGTCC 1010
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