Tag | Content |
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EnhancerAtlas ID | HS184-15171 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:9165290-9166620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr19:9166157-9166169 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr19:9166511-9166532 | ATTTTCTTTTTCTTTCTCTTT | + | 6.58 | IRF1 | MA0050.2 | chr19:9166517-9166538 | TTTTTCTTTCTCTTTTTCTTT | + | 7.4 | RUNX1 | MA0002.2 | chr19:9165761-9165772 | AAACCACAGAG | - | 6.14 | ZNF263 | MA0528.1 | chr19:9165847-9165868 | TTTCTTTTTTTTTCCTCCTTC | - | 6.08 | Zfx | MA0146.2 | chr19:9165925-9165939 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 9165361 | 9165882 | chr19 | 9166059 | 9166497 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I009052 | chr19 | 9163305 | 9167024 |
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Enhancer Sequence | TTTTCCAAGC TGGTATCGAA CTCCTGGGTG CAAGTGATCC TCCCGCCTCC GCCTCCCAAA 60 GTGCTGGGAT TACAGGTGTG AGCCACTGCC CCCAGTTCCT TCTCTCTCTT CTGTCTGCCG 120 CTTCTCATCC CTTCCACCCA ACCAGGGCGG GAGAGGGAGG GGGATGAAAC CAGGACGGGG 180 AGGTGGGAGA GGGATGAAAC CAGGGCGGGG AGGTGGGAGA GGGATGAAAC CAGGGCGGGG 240 AAGTGGGAGA GGGATTACAA ACTCCCTCTA TTTACTCTCA AGCTTCTCTG TTTCCACCTC 300 CACTAACCCT GGAACCCTGA GGCGCCCCAG GCCTGCAGTG TATAAATGCC TTCCTGGCAG 360 GCCTTGCTGA GACTTGAGCT CAGCAGTCCT CACCCTCCTT AATCCTAACC AAACAGGATC 420 TGTCACTAGG CTCAGCGTGC AGAGGACGCC TCGGGTCCTT TTCCTCCTGC GAAACCACAG 480 AGGCAGCCCT AGGGGCAAAC AATAAAACAG TGTGGAGGGC TGGGGGATGA GGGTGGGAGC 540 ATGCCTGGCA GGGAACGTTT CTTTTTTTTT CCTCCTTCAA AAATTGGAGG GGAGGCCTGG 600 CGCGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGC GGATCATCTG 660 AAGTCAGGAG TTGGAGATCA ACCAGACCAA TATGGTGAAA CCCCATCTAT ACTAAAAATA 720 CAAAAATTAG CCAGGTGTGG TGGTGGGAGG CTGTAGTCCG AGCTACTCAG GAGGCTGAAA 780 CAGAAGAATT GCTTGAACCC GAGAGTTAGG TGGCAGTGAG CCGAGATCGT GCCATTGCCC 840 TCCAGCCTGG GTGACAGAGT GAGTCTCAAA CAAACAAACA AGCAAAAAAA AAAAAAAAAA 900 ACAAGGAAGG GGATCAAAAC TGTCAGTTGG GACAAATACA GGCTTTACTA TGGTAATTCT 960 CTGGCTTTGA GCCAAGGACT GCACCCTCCC CAGGGGGCAG CGCTGAGAGC TAAGTCACCC 1020 AGGATGGTTT AAAATTAAAC TCAATTTTCA ACATTGTAAC TCCTCACAGA CAAACACAAC 1080 TGTGTTTACT AATAGCATTT CTCGGTTTTA TCTGACTTTT GAGTTCTGAA GTCGGGAGAT 1140 GTGGAGGCTG GAAGTATAAA CTGAGACGAA GTGGGCAGAA CAGCTCCCTC CCGGCTTCCC 1200 CATCCCCAGC CAGCCTCTCT GATTTTCTTT TTCTTTCTCT TTTTCTTTTT TTTTTTTGAG 1260 ATGGAGGCTT GCTCTGTCAC CCAGGCTGGA GTGTAGTGGC CCGATCTCAG CTCACTGCGA 1320 CCTCTGCCTC 1330
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