Tag | Content |
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EnhancerAtlas ID | HS179-26152 | Organism | Homo sapiens | Tissue/cell | SkMC | Coordinate | chrX:101914420-101915400 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chrX:101914564-101914576 | GAATGTTTGTTT | + | 7.22 | GCM1 | MA0646.1 | chrX:101915247-101915258 | GATGCGGGTAC | + | 6.14 | MITF | MA0620.2 | chrX:101914857-101914875 | GTGGGTCATGTGACCAGG | + | 6.09 | MITF | MA0620.2 | chrX:101914857-101914875 | GTGGGTCATGTGACCAGG | - | 6.09 | Myod1 | MA0499.1 | chrX:101915173-101915186 | AGCAGCTGTTGCT | + | 6.59 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTCATTATA AATGATATAA ATTAAATTCC AATATGATGT TAGTTTGCTA AGGTTTACGA 60 AAGCAGGGCA AAGTGGCAGT TTTGCCTCCC TTCACAAATC AAAAATTTTA ACAGGGATCA 120 TCCTGGTGGT GCAAATTGGA GTTTGAATGT TTGTTTTGCT TACCAGCATT TTTCAAGACA 180 GATCTTGCGT GTGTTTTAGT ATGTCGCTCT AGTCGTATAC AAAATATCAC AAATCACTTC 240 ATCTCCCCAA TCCTCATCGA ATGTTCCTCG CCAGCCCAGT GGTCCTCCAG AGCAAAGCCC 300 GGCCTTCCTT CCAGCTGTCT GGGCCAGGAG CTTGAGGGTC TTCTAGCAAG CACCCCGGAG 360 GCTGTCTTCT GACTGTCATG CAGGGCTGTG GCAAACTAGC TGACTGCGCA GTCACGTGGA 420 GGGGGGAGGG GCTGACGGTG GGTCATGTGA CCAGGCTCTG GGTTGAGCCG GCCTAGAGGA 480 GTGTTTTCTT ACACCCAGAA AGTACAGGAA AGGCAGACGA CAACTGTGCT CCGCAGAGCG 540 GGAGGTGGGG GGAACGGCGG AATATTAAGG TGGGTAGGTG TCTCTCCATG CTTCATCAGC 600 CTGAAAACTA ATTTCTCAGG CGACCGGAAT TACAGCATTT CTTGGTAGAG GAAACTATCC 660 CTCAGCCAAC CGCTAGCGGT CTTAGACGGT CTGTCTTTTG TCCAGGAGCT CAAGAAGCAG 720 AGACTCTACC TGCCCTAGGC GTTCGTGAAG AGAAGCAGCT GTTGCTATTG GAGGAGGTGG 780 GTGCAAGGAC GGCAGATGCC ATCCCTGAGA GGCGGTGACT GAGACTAGAT GCGGGTACAG 840 GTAGTGCCTC GGATCCCCGG GCTGCCTCCT GCCTTTTGAA CATCCCAGGG GTCCCAACCC 900 AGCGCCCTGT GTTTCTATGT GTGGGTGGGA GAGGTGGGCA TATGGATGGA GTTGGCTTCA 960 GGGGAGCCCA GAGAGGGGAA 980
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