Tag | Content |
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EnhancerAtlas ID | HS098-24111 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr17:42658820-42659950 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:42659133-42659148 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr17:42659133-42659151 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 42659497 | 42659593 | chr17 | 42659365 | 42659489 |
| Enhancer Sequence | GTGTCTCACT CAGTCGCTCA GGCTGGAGTG CAGTGTCGAT CATAGCTAAC TGCAGCCTCG 60 AACTCCTGGG CTCAAGCAGT CCTTCTGCCT CTATCCTCCA AAGCGCTGGG ACTACAGGTG 120 CACACCAGGG CACCCAGCTC ATCCTGTCCT TTCCAAGGCT CTTGCAGCTC CAGCATCATA 180 CACTGTTTTT TTCTCTCTGC GTTTCTTTAA AGAGGATGCA GTGTTCCCTG AAAGAATCCA 240 CCACCCTGGC CAGGCGCGGT GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCGAGGT 300 GGGCGGATCA CCTGAGGTCA GAAGTTCAAG ACCAGCCTGA GCAACATGGA GAAACCCCGT 360 CTCTACTGAA AATACAAAAT TAGCCGGGCA TGGTGGCTCA TATCTGTAAT TCCAGCTACT 420 CGGGAGACTG AGGCAGGAGA ATCACTTGAA CCCAGGTGGC CAAGTTTGCA GTGAGCCGAG 480 ATCAAGCCAT TGCACTCCAG CTTGGGCAAC AAGAGTGAAA TTCTGTCTTA AAAAAAAATC 540 CCCCACCCTG TCACCTCCCC CCGAGCCCTG CACAGCGCAT GCTCACAAAC AGCAGCAGGG 600 GGTGCTGTAG ATGAACACAC AGGCACTGCC AGGCGGGCAC CCTGTTGGAG GAATCTCCAT 660 GGCACTTGCT GCTGCTGATT ATTATTATTA TTATTAGACA GGGTCTCGCT ACGTCGCCCA 720 GGCTGGAATG CAGTGGTGCG ATCACAGCTC GCTGCATCCT CAAACTCCTC GGCTCAGGTG 780 ATCCTCCCAC CTCAGCCTCC CAAGTAGCTG AGACTACAGA CAGGTATGTG CCACCATGCT 840 GGGCTAATTT TTTACTTTTT GTAGAGGTGG GGTCTCGCCA GGTTGCCCAG GATGGGCTCA 900 AACTCCTGAG CTCAAGCAAT CTGCCTGCCT CAGCCTCCCA AAGTGCTGAG ATTACAGGTG 960 TGAGCCACTG CAGATGTTTT TTTAGCAAGT ACCGCTTGTA CGTAGTATAA AATTTAAAAG 1020 GTACAAATGA ATATGCAATG TACCTGCCTC CCAGCTGTGC AGTTCCCCTT CCTGGAGCAA 1080 GCTGAGGAAG TTTTGTAGTG TTTCATTCTA GAGACAGTTT ATGCTTATAT 1130
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