Tag | Content |
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EnhancerAtlas ID | HS183-08554 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:936070-937530 |
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) |
Gfi1b | MA0483.1 | chr7:936225-936236 | GGCTGTGATTT | - | 6.02 | REST | MA0138.2 | chr7:936356-936377 | GACCCTGTCCTAGGTGCTGAC | - | 8.06 | RUNX1 | MA0002.2 | chr7:936737-936748 | TTCTGTGGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41630 | chr7:936595-937921 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr7 | 936682 | 936727 | chr7 | 936295 | 936576 | chr7 | 936738 | 936818 | chr7 | 936844 | 937277 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I000897 | chr7 | 936961 | 937985 |
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Enhancer Sequence | GGCTGTGCAA CGCTGGTCCT TTCTTGGGCG CTGGTGTGGG GGATCTCTCT CTGCTCTCAG 60 GGCTGTGCCT GGGAGCCCCC AGAGGAGGCG TACCCTGTGG CCAGACTGCC CGTGCGTGGA 120 CGGAGCAGAG GGCTATCAGG AAGTCACGTT CACTTGGCTG TGATTTTAGA AATAAGTTTT 180 GTGTAATTTC ATCAAAATTC ATAAAAATCA AATCCACCAG GTCTGGGTGT CACAGCCTCA 240 AAGAGCAGGC CCTTGGGCTG CAGGGGAGAC AGTGGCGCAG AGCCCTGACC CTGTCCTAGG 300 TGCTGACAGG ACACCCGTCC CTCCCGTGTG GCACTTGCTT TGAGCAGCGA GTTCGATCCG 360 GAGTGACCAA GGATTTTGTG TGCGGCGTCA CTCGGGCTTA CCGTGAGACG GCAGGAACAG 420 CCGGCCGGAG CCCCGCAGGC GGCCCCTCGT GGCCCGTGCT GAGCCTGCGC CGCGGCGTCT 480 GCCTCTGCCT GCCTCAGGAC TTCGCGGCGG AGTCACGGTC CGTCCCTGTG CCTGCTGCCA 540 GCAAGGGGAT GCCCTTCCCC ACAGCTGTGT CCACGCGGGG AGGTGTGGAC AGCGAGTGAG 600 CGACCACCTT CTGTGCCTGC GCCACCTCCC CTGGTTCAAA AAATTCTTTC CCCCCATTAG 660 AAAGTTGTTC TGTGGTTTTT AAAATGTGAC AGTCGTCAGT GTCCTCAGCA CACACGTGGA 720 CACGTGCACA TTCGGGGACA CGCACACACT GAGCACGTGC CCACACTTCC ACGCCATGGG 780 GAGGGCTGTG GGCACTGCTG GTTTCCCCCG GGGGTGTGTC CAGCACAGCC CAGGGCTCTC 840 CCTGACCCAG GCCCACTCCT CTCACCTCGG GTTAGGACCG TGGCACCTGG TGAGGTTGCG 900 GGGCACTTGC CTGGGGTTTC AGCTCCAAGT GGGGGTACCT CGCCCACATC CTCGTCACCA 960 GCACAGCTGC CTTGGGGACC CCTAGGCTGG GATTGGGAGA CCTCTACTCC GCCCTAGAGT 1020 CCCAGCTCCT CATTGGAGAA GTGGGATTCA GCATGTTCTG TGTGAGGGCT GAGGGGCCCA 1080 GCATTGGGGG GGTGGGCTGG CAGGCACAGG GGACCCCCGA CCCGGGATGC ATCCCCCACA 1140 CTGTCCTTCA TGCTGAGCTT GGCTTGGCTT TCAGGCTGTG GACTCTGCCC AGGAACTGCC 1200 TGGCGGGCCT CAGATGGAGG GGGCACCTGG GGAAGGGGGG CACCTGGGGA AGGGGTGCTG 1260 GGGGGCACCT CGGGTAGGGA CCGTCTCCCG TGTACAAGGA GCATGGCGCT GTGACTAGCT 1320 CAGACACCGT GTCCTCCCTC CAAACCTCAG GGAGCGAGGG CCCTGTCAGG TCCCTGGGAG 1380 CAGACGAAGA TTCTCCTGAA GCCAGGGAGG CAGGGCCACG TGTTCCCAGC CCAACTTCCT 1440 CCCCACTCCA TCCTCGGACA 1460
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