Tag | Content |
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EnhancerAtlas ID | HS184-07694 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:54342190-54343710 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr12:54343512-54343527 | AGGTCTTTCTGACCT | - | 6.33 | ZNF263 | MA0528.1 | chr12:54342231-54342252 | GAAGAAGAAGAAAGAGGAGGA | + | 6.38 | ZNF263 | MA0528.1 | chr12:54342237-54342258 | GAAGAAAGAGGAGGAGGAGGT | + | 6.3 | ZNF263 | MA0528.1 | chr12:54342240-54342261 | GAAAGAGGAGGAGGAGGTGAA | + | 6.4 | ZNF263 | MA0528.1 | chr12:54342249-54342270 | GGAGGAGGTGAAGAAGAAGAA | + | 6.69 | ZNF263 | MA0528.1 | chr12:54342234-54342255 | GAAGAAGAAAGAGGAGGAGGA | + | 7.2 | ZNF263 | MA0528.1 | chr12:54342243-54342264 | AGAGGAGGAGGAGGTGAAGAA | + | 7.39 | ZNF263 | MA0528.1 | chr12:54342246-54342267 | GGAGGAGGAGGTGAAGAAGAA | + | 7.86 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 54342506 | 54342600 | chr12 | 54342600 | 54342800 |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I053948 | chr12 | 54342781 | 54342930 | GH12I053949 | chr12 | 54343421 | 54343570 |
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Enhancer Sequence | ACCGAGACTC TGTCTCAAAA AAAAAAAAAA AAAAAAAAAA AGAAGAAGAA GAAAGAGGAG 60 GAGGAGGTGA AGAAGAAGAA AAAGGAAAGC CTGTGCAGGC TCACTACTGG TGCATTGGGA 120 CACTGGTAAG CCTAAAAAGG ACCTCAGTTC CTGAGTGCCT GTGAGCCCTC GTGCAGTGCA 180 TTAAATATAC CCAGATTTAT TTTGGAGGAG TATCATGCCT GGACTTATTT GGATATGACT 240 TTACCATAAG AGTAAGCAAA CACTGTGTGA GTGTGTGTGA GCATGTGTTT CGGGGAGGCA 300 CATTTGTGAA ATATATTATT CTTTCCCTGA ATAAGGATTT CTTCTTTAAC ACAACTCTGG 360 TTGTGTTGAT TTCTTACCTT TCCTTCTCCC AAGAATTGGC ATTGTCTTTG GGGACTCTAT 420 GAGATAGTTC ATCTCTTAGT CATGTCTCTA ATATGTCTTT CTCTCCAAGG CCAGCCTCCT 480 AGTGTTTGTG TTAAAAGTAA GACTAAGTGT GAAGGCAAAT ATGAGGATAC CGGGGGTACA 540 GGGTGATCTG AATTGCTGGT GAAACCTCTG TGAGGAAACG CAGACACACA GAGGGGCTGA 600 GACTCCTGCT ATCTTTCTCA TAATCTGATG GTACTCCCCA CTTCCCCTAT CTCCCTAGGC 660 CAGAGCTGGG AGGCCCAGGC AGCCAAGGGC CTCACAGGAC TCTCCATCTA GTGGTCACTC 720 TCCGGGGCTG CCAGAGAGGG CTTCAAGAGA TTCTTTGCTG AGCTTGGGGG AAAAACCCTT 780 CCCCACCCAC ATCTTAGTCT CCAGACAGAG GCCCAGCAGA ATGGGCCTTT CAGCCAGCAG 840 TCCCACAGCC GGAACCCAAC TGAGAGAACA AGGGCAGCAG TTCTTTCCGC AGATCCCTCC 900 ATGACTGTCT GCTCCAGAGA CCATCTGCTC CTGGGGTTGA TCCACAGGCG GCTGGGTGAG 960 CAATGTGGGG ACAGTAGGCC AGTGTGGGTG CAAGGCAGGG GCAGGCCCCT GGGGCAGCCG 1020 CTATCTCTCT GAACAGCCCT CCTATTGGAG GTGGGGTCCA TGCGGCAGGC AGCCCCTTCA 1080 GTGGCTCCAT CTGTTCAAAA GAGAACTCCC CACCCTAGGA TCTGCTGGGA TCTGTGTTGG 1140 GTGGTATTGG AGCCCACCCC CAAGAAAACT CCAAGAGTGG TTCAGGCAGA TGTATATCTA 1200 GACCTGCACT GGTGGAGAAT TGAGGGGCCC TGGGGAGCTA GGGACTTCTG GGAGGAGGAG 1260 GAGGGGGCCA GAGCCTTTTC AAAACCAACC AGGCTCTTCC TCTTTTAGCC TTGACCGTGA 1320 CTAGGTCTTT CTGACCTTGA CATCACAGGG AGCACAGGGA AGGGGGGGGA GGGGTGGAAA 1380 AGGCCTTGAT CTTCCGGTGG CCAGCGAAGG GGAGGGCTGC TTGCCCCCTT GACGCGCCAT 1440 CCCCCTTCCC GCAGGAGCCC GCCGCCTCTG TTTACACACA GAGGAGGTGT CGTCTCCAGT 1500 CTAGACAAGG GCGCTAATAA 1520
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