Tag | Content |
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EnhancerAtlas ID | HS046-16064 | Organism | Homo sapiens | Tissue/cell | Fetal_muscle_leg | Coordinate | chr17:75953910-75955000 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr17:75954899-75954911 | CGCCCCCTGACA | - | 7.22 | SP4 | MA0685.1 | chr17:75954561-75954578 | GGAGGAGGCGTGGCCTG | - | 6.14 | YY1 | MA0095.2 | chr17:75954795-75954807 | CAAGATGGCCGC | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATCACGGCG GCGTACGGAG CACCGGGGAG GAATCGTGGG GTGCGTAGGC GCCGGAGCGC 60 CCGGGTTCGG CCCGGACCGA AGGCTTGCGC GGTGAAGGTG TGGTGTCTGT GCTCCGGGGA 120 AAGGGCTGTC TCCCCGGGGG ACTGTTTCGC AGCGAGGCTT GTTTTGCTCG CAGCTGGGCG 180 CTCCCTGGGG AGCGACTGAG CGCAAGGGCG GGCCGGGAGG CGCGAGGCGA GCACGATGCT 240 CCAGGGCCCC AAGGACTCGT GTGCGTGTGC GTGTGCAAAG TGGGGCGGTG CAGGGCGTGT 300 GCACGGCACG GGCGAGACGC GCGCCGGTGC GGGCGCCGGG CGCCGCCGGG CGCAATTACA 360 GCATAAAGCC CGGGCGCCGC GGGGCGCTGG CCCGGAGAAC CCACCGGACG CGCAGAACCG 420 GATCGGCACC CCTCCCGCCA GCACCCTAAC GCGGAGCCAC AGCGCCCAGG GACCGGAGGG 480 CAGGCGGCGG CGGTAAAGGA CACCACGCAA GTCTCCACGT AACCCCCCCG AGCAGTGCAA 540 GCTCCCAGGA CTGGCGCGCG TCCCGGCCAC TCGGAGCGCG CACCGCTCGC ACCCCGGCGC 600 GCTCCCCGCG CGGTGCAGGG AACCACAGCG CGGGCGGGTA TTAAGGGGAA AGGAGGAGGC 660 GTGGCCTGGC CGAGGAGCCA ATGGGCCGGG AGGGGCGCGC GGGGGAGGAG CTCAGGTGCA 720 GAGTGCCGAT TGGCCAGTTC GCCCTCCGGT ATGCAGATAC GGTGGGAGTC ACGTGCTAGG 780 GGCCGGGACG ACTTCCTGTT GGAGGCCAAC GCGGGGCGGG GAAGGGGGCG CGAGCGCCCC 840 GTCTGGCTGA AGCGGGGGGA GGGGGGTTCT TGTCAGTTAG AGCAACAAGA TGGCCGCGGT 900 GGCAGCTCCG CACCTCAGCG CGACGGCCCC GGGAGCCGTA GCCGCCGCCG CCGGCCCCGC 960 CGCCGCGCAG TCTTGAGCGC CGCCCGGGCC GCCCCCTGAC AGGGCAGTCC CAGCGCCCGC 1020 CGCGCTCCCG CCGCCGTCAC CGTCGCAGTA GCCGCGGGCC CGCCCGAGCC GGAGGCGGAG 1080 GGAGCGGAGC 1090
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