Tag | Content |
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EnhancerAtlas ID | HS133-06857 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:6202070-6203420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr12:6202927-6202947 | GCCCCAAACACCCACACACA | + | 7.13 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27167 | chr12:6201932-6203586 | Esophagus | SE_37940 | chr12:6196664-6208010 | HUVEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I006092 | chr12 | 6201824 | 6203813 |
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Enhancer Sequence | CATAGCTCCT CCCATAACCT GTTAAATATG TACACTGAGC CAACCCTTTT GGAATAAGTT 60 TCTATTCCAC CCCTTTCTCC CTTGAAGTGC CTGCTTTCAG TTTCTACCAG AGGCTACACT 120 TCCCAGCCTG CAGGATGGCC AGCCTGCAGG CCACAACTCT GAATAAGAAA AGCTCTCCTC 180 TCTAAGTTTA TGAACCTTGT GATTCTTCAG TTGACATTTT TGACAGTGTG GTTGCTCTCT 240 GGATAAGGGC AGGAAGGTGG TGCTGTCAAG CAGAGCAGCT TTGTAGAGGG TGTCGGGGCA 300 CAGCGTAGGT GTCGGGGCAC AGCGTAGGTG CCCATTCAGA GCCCGAGGAC TCATCCACCA 360 GCTGTCCAGT GTTGGCTGCC AAGGGCTCAC CACTGAGTCA TTCCTCAGGA ATGGCCCTCA 420 GCCCAAGGGA GTTCCACCTC CTTACCCAGG GCAGCCCACA TCCAGTGACC AACAGGGGCC 480 ACTCCACCTT CCAGAGCTCC TTGAAGGATC AGCTGAGGCC CCGCTGAAGC TCTATCAGTG 540 CTATCACAAG CAGTTCAACT TCTCCCACTG CCCAACTCTG CTTCTCTCAC TTCCTAACCA 600 AGGCTGCTCG AGAGCTCCCC AGTAAACCTC CTGCATACAA ACGTCCCGCC CAGGGAGGCT 660 GACTCACAGC ACCACCAAGG AACCTTGCTC CTCAGATGAT GAGTCTCTGA GCACAATCCC 720 AAAAGGGCAA CAACCCCTGT TCCCCACAGG AGTCCAGCTT CACAGCTGCA CCTACCTCCT 780 CAGCCCAAGT CAGCCTGTTC CACAGTGGGG AGGGAATTAC CCATTGAGTG AGGTCTTGCC 840 CCACATAAAG CATTCTTGCC CCAAACACCC ACACACAGAG AGGCACAAAG ACCATCTTTA 900 CCTGTGGCAG GTGAAGGCAG AGTGTGGTCT GGCCACCCCT CCCCACCTCC CCTTCTCTCC 960 AGTGTGAGGT CCTGGTGAGT GAGATCATGA ATGGCAACTC TGATGCAGAC AGAGCTGCTA 1020 CAAGGCTACC TTGTAAGTGG CAACAGGGCT CTGTGGAAGG GGTGGGGCAG TCCTCCCAGC 1080 CTTGTCAGGG TTGGCAGGCA TTAGCACACA CAGGAGAGGA GAAGGCCATG TGACCACAGA 1140 GGCAGAAATT GAAGTCATGA GCCCAAAGAC AGGGAATGCC GCTGCCACCC AAAAATGACG 1200 GAAGCAAGGA CCTAGAGCCT CTGGAAGGAG CAAAGCCAGC CAACACCTTG ATCTCAGCCC 1260 AGGGAAACTA AATTTGGACC TCCAGCCTCC AGAACTGGGA GAAAATAAAT GCCTACTGTT 1320 TTAAGCCATT GAGTATGAGA TAATTTGTTA 1350
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