Tag | Content |
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EnhancerAtlas ID | HS105-17376 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:6202110-6203520 |
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 | CAACCCTTTT GGAATAAGTT TCTATTCCAC CCCTTTCTCC CTTGAAGTGC CTGCTTTCAG 60 TTTCTACCAG AGGCTACACT TCCCAGCCTG CAGGATGGCC AGCCTGCAGG CCACAACTCT 120 GAATAAGAAA AGCTCTCCTC TCTAAGTTTA TGAACCTTGT GATTCTTCAG TTGACATTTT 180 TGACAGTGTG GTTGCTCTCT GGATAAGGGC AGGAAGGTGG TGCTGTCAAG CAGAGCAGCT 240 TTGTAGAGGG TGTCGGGGCA CAGCGTAGGT GTCGGGGCAC AGCGTAGGTG CCCATTCAGA 300 GCCCGAGGAC TCATCCACCA GCTGTCCAGT GTTGGCTGCC AAGGGCTCAC CACTGAGTCA 360 TTCCTCAGGA ATGGCCCTCA GCCCAAGGGA GTTCCACCTC CTTACCCAGG GCAGCCCACA 420 TCCAGTGACC AACAGGGGCC ACTCCACCTT CCAGAGCTCC TTGAAGGATC AGCTGAGGCC 480 CCGCTGAAGC TCTATCAGTG CTATCACAAG CAGTTCAACT TCTCCCACTG CCCAACTCTG 540 CTTCTCTCAC TTCCTAACCA AGGCTGCTCG AGAGCTCCCC AGTAAACCTC CTGCATACAA 600 ACGTCCCGCC CAGGGAGGCT GACTCACAGC ACCACCAAGG AACCTTGCTC CTCAGATGAT 660 GAGTCTCTGA GCACAATCCC AAAAGGGCAA CAACCCCTGT TCCCCACAGG AGTCCAGCTT 720 CACAGCTGCA CCTACCTCCT CAGCCCAAGT CAGCCTGTTC CACAGTGGGG AGGGAATTAC 780 CCATTGAGTG AGGTCTTGCC CCACATAAAG CATTCTTGCC CCAAACACCC ACACACAGAG 840 AGGCACAAAG ACCATCTTTA CCTGTGGCAG GTGAAGGCAG AGTGTGGTCT GGCCACCCCT 900 CCCCACCTCC CCTTCTCTCC AGTGTGAGGT CCTGGTGAGT GAGATCATGA ATGGCAACTC 960 TGATGCAGAC AGAGCTGCTA CAAGGCTACC TTGTAAGTGG CAACAGGGCT CTGTGGAAGG 1020 GGTGGGGCAG TCCTCCCAGC CTTGTCAGGG TTGGCAGGCA TTAGCACACA CAGGAGAGGA 1080 GAAGGCCATG TGACCACAGA GGCAGAAATT GAAGTCATGA GCCCAAAGAC AGGGAATGCC 1140 GCTGCCACCC AAAAATGACG GAAGCAAGGA CCTAGAGCCT CTGGAAGGAG CAAAGCCAGC 1200 CAACACCTTG ATCTCAGCCC AGGGAAACTA AATTTGGACC TCCAGCCTCC AGAACTGGGA 1260 GAAAATAAAT GCCTACTGTT TTAAGCCATT GAGTATGAGA TAATTTGTTA CAGCAGCTTC 1320 AGGAAGCCAT CCTGACATCC AAGCTATGTC ACTTCAGGCA CAGCCTCTCA CTCAGACTCC 1380 CTTCAGTGTC TGCAACTATA AAGTAGTTTT 1410
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