Tag | Content |
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EnhancerAtlas ID | HS059-06866 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr10:112295600-112296780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr10:112295945-112295965 | CACCCACACACACACCCCCA | + | 6.17 | RREB1 | MA0073.1 | chr10:112295941-112295961 | CCCCCACCCACACACACACC | + | 7.19 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_34496 | chr10:112295716-112296656 | HCT-116 | SE_46068 | chr10:112295378-112297015 | Osteoblasts | SE_56127 | chr10:112295384-112297030 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 112295837 | 112296727 | chr10 | 112295745 | 112296221 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I110535 | chr10 | 112295559 | 112296757 |
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Enhancer Sequence | CTCTTATAAG CCATGTACAT GTAACATCTC ACTTGATTTT CGCAGTGACC CCATTCATGG 60 ATTCTACTAG TATTCTCATT ATATTGTTAA GAAAACAGAG GCTCAGAGAA GTAAGGTAAC 120 CTGTCCAAAT GGTTGATCGA GTAAGCAAGG TTCCCGACTG CAGGAAGGCA GAGAGATGCT 180 GCCTCCTGGG GGCTGTCCCT TTCTACAGAG AAGCATTTTC TTCATGACTG AGATCGGGGG 240 TGGCCCCAGT TCCCTGGAGA CACCAGTGTT GCAGGAGGCT ACTCTTCTTC CTGATTTCAC 300 TGCCCAGTTC TGTGGCAGCT CCAACCCATA ACTTGAATGT CCCCCCACCC ACACACACAC 360 CCCCACCTCA GCACAGTGAC TTTCCCCCAA GGCTGTGTCA CGCTTAACAG ATGACACTCA 420 GGGAAAGGCT CTGTGGTTGA ATCACAGTGA CCACTTCCTG TTCCATTCAG GGTCCCTTGT 480 TCTCCAGAGC CCTCACTCTG CCATGCCCTA TTTAGTAAAT GCCACAAAGT TTATGACTCC 540 TGGACTGCTA GGGGGGCTTA GTCACCCCTT CCTATACCCT GATTCTACTA GACTTAGAAG 600 CATCAACTCT CAGTTTCTGC ACCATTTCAC TACCTTGCAA CAGGAGCCTG GTGGGACACC 660 CCGTTTGTCC CGGGGCTGCA CAAGTAGGCA AAAGGACGAT CTCCATTCCT CTAGACTGGT 720 GATGTAAGGC TGACCGGACA GGTGGGCAGA CGTCCAAACC TCAGCCATGA AGTAAGGGAG 780 GTAGTCACTG ACCCGGTGGG CTCCTCAGAG GCACCTACTC ACTGGATGTT GTTGTCTGCA 840 AGCACATGGG TCAGAACACC AAGTGGAAAG AAATGCCAAG GGGTTTATAT GTCTTTGAGG 900 GAAACCCCAA TTCTCTTTCA TTTGCTCAGA AATGCCTTCC TGGAGGCTGA CAGCTGTAGC 960 TAATGTTGAG TCCTAGAGCC GAGGGAGTCA TTAGATACTA GGGGGCCATC CGGAAGAGGA 1020 GACTTCCTCT GGGTAAATGC ACAGAGCAAA ATCTGGGACC ATCATGGCTG GATTAAGATC 1080 TTTAGCAGTA CTCAACCTCT AAAGATTATG CTACAAGTAT TTCTTGCCCC ACACAAATCA 1140 TCATAGATAA CATAAAATAA AACAATCTAA ATCCTAAAAA 1180
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