Tag | Content |
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EnhancerAtlas ID | HS183-09406 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr7:43152530-43153750 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr7:43152662-43152683 | TCCCCACCCTCTCGCTTCTCC | - | 6.07 | ZNF263 | MA0528.1 | chr7:43152572-43152593 | CCTTCCCCCCCGCCCTTCTCT | - | 6.41 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCAAGGTAA GCGGGCGTAG CGCGGGGACA CTGTCTGCCG CCCCTTCCCC CCCGCCCTTC 60 TCTGGGCGGC TTCCCCGCCG CACGCGAGGC CCCGGCAGCG CCCTCCCTTC TCGGGGCCGA 120 GATCCACCCT CCTCCCCACC CTCTCGCTTC TCCCGCGAGG TTCAATTGTC AGCCTGGGTC 180 GCGCCGCCGC CCGGTCCGGG CCGGCATCCC CGGGTGGCGA CCCCGGCTTG GGTACTGCAG 240 GCGCACCCGG CCCTCCTGCG GGGTACGGAG AGAAACAAAG AAGCCCCCAA GCGGGTTCGC 300 AGCGCCTCCC CCGCCCCTCA GCGCCCTCCC AGTGGCGAGG AGGTGTCAGG GGAGGGGGCG 360 GAGAGACCTA CGTAATCCCC CTTCCCAGCC CACACCCACC CCTTGTGAAC CAAAGCTCTG 420 GATTTGCGCT TCGCCTTGGG CTCGCTTTTG AACAATTGTG TCCCATGCAA TGCCCGTGGT 480 TAGCCCAGAG AGCGCCCAGA GCCTCCGCAC GGGCTCGCCG GTGCTCGCTC GAGGGGCGCG 540 TGGCCAGGTC CGGCCCTTGC TCCCATGGAC GGGTGCAGGA GGGGAGGAGG CGCTGTGTGG 600 GTGCTCCCCC AGCGCCTCCC TGTTACCGGC CGGCTGCGCC GCTCAGCCGG GCCTGCCACC 660 TGAGTTTTAG CGGGAGCAGT CATGTCGCCT ACCGTATTGC GACTTGCAGA CAGGCAGGGA 720 GGGAGCTGCC GGGGCGGGGA GGGGGGGGGA ATGCGTCCGG TCCATTTTTG GCTGGAGGTG 780 CGCTTCCTGC TACCCCCACG TTCCCGGGCG GTGACAATGC AGCAAAATCC GAGGGCTCAA 840 ACAATGTGGC CCCTCCATCC CCGGCTCCAG GGCATTCTGA TTGCTCTGCC GCTTTGACGT 900 CCCGGCCACT TGGCTGATTT TCAGAGCCAT GATGCGCGGT GTCTCTGTCT TGCACACAGA 960 GGCTGGGCAC CATAACTTCT TCCCTGCCGA ATTTCAGCGC GTAGGGGGAG CTGGCAGGGA 1020 CACAGGCTGC AGAGATGCCC GGCTTCCTGT GGTTCCGGGC ACAGCGCGCC TCAGTCTGCA 1080 TTGGGCTGAC ACCAGAGAGC ATGTGGGGAT TTTCCTAGTT GCCGAAGAAG ATATTATTTG 1140 ACGTTGCTGT AGTTTTGTGC TTACTTCTCT TGGAATCTGC AGTGGTGCAA TTCTCCCCTT 1200 GTTTTCCCCC CTTCTCTTTG 1220
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