Tag | Content |
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EnhancerAtlas ID | HS183-13684 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:130576360-130577290 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr9:130576707-130576722 | GAGGTCAAGAGGTCG | + | 7.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTTGACCC CCTGCTCCCT CAGCAGAGAC GGAGGGAGGG GCTGCTGGTG GTCAGGGACC 60 TGCACTGTGT AGAGGGAGCC TGGCTGTGTG GCCTGGAACA AGTCCCTCCC TCCCTGTGCG 120 CCTCAGGTGG CCTGTCTGTG AGATGAGAAG AAGACCAGAC TGAAGCCTGT TCACCATATG 180 CCAGGCAGTG CTTTCTGCAG ACCCCCTTGC AGAGACCTTG TGATGGAGAA TTATACACAT 240 TTGACAGACG AGGGAACTGT GGCTGGTTTC AAGAAGCCAT GGAGGCCGGG CACGGTGGCT 300 CACGCCTGTA ATCCCAGCAC TTTGGGAGGC TGAGGCGGGC GGATCATGAG GTCAAGAGGT 360 CGAGACCATC TGGCCAACAT GGTGAAACCC CGTCTCTGCT AAAAATACAA AAATTATTAG 420 CTGGACGTGG TGGCGCATGC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGACAATT 480 GCTTGAACCT GGGAGGCAGA GGTTGCAGTG AGCTGAGATA GAGATAGTGC CACTGTACTC 540 CAGCCTGGGC GACAGAGCAA GACTCCATCT CAAAAAAAAA AAAGCCATGG GACCTGCCTA 600 CAGTCACAGG CCAACAAGGT GGCAGGTCCA GGATTTGAAC TTAGAGCAGT CGAGGGCCTG 660 TGTTCGGAAC CCCAGAGTGA GAGTGTGGAT GGGGCCTCCT GGTGTTTGCT TTCTTGCAGC 720 CTAGACCCTG GGGTGTGCTG TCGAGTGGGT GAATGGCAGA GGGGAACTGG CTGAATGAAA 780 ACCTGCTGTG CCCTGGATGC TGCTACTGTT CAGGATGCCA CCCCTGCCAC CAGGCCAGCC 840 CAGTGGGGGC CAACTACAAA AGCAGCCCTG TCCTGTGCCC TCACCCCACC CTGGCTTTGA 900 ATGTCACTGC CCTTCTCCCA GCCCAACCCA 930
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