Tag | Content |
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EnhancerAtlas ID | HS105-14698 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:66659060-66660140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr11:66659829-66659840 | TGTGACTCATC | + | 6.14 | JUND | MA0491.1 | chr11:66659829-66659840 | TGTGACTCATC | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr11:66660099-66660114 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr11:66659081-66659096 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr11:66659674-66659689 | ACTGGCCTTGAACTA | - | 6.5 | ZNF263 | MA0528.1 | chr11:66659566-66659587 | GGAAGAGGAAGGGGAAGGAGT | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_00471 | chr11:66658889-66660128 | Adipose_Nuclei | SE_34512 | chr11:66658992-66660885 | HCT-116 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 66659412 | 66660070 | chr11 | 66659730 | 66659912 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I066891 | chr11 | 66659143 | 66660981 |
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Enhancer Sequence | CCACGTTGGT CAGGCTGGTC GTGAACTCCT GACCTCAGGT GATCCACCCA CCTCAGCCTC 60 CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCGCACCCAG CCAATAGGCA AGTTTTTAAT 120 ATCAATATTG CCAAATAAGT CTCAAGGTAG TTATCCTAAT AATTTACACA GCCACTAGAA 180 ATACAACAGA ATGTCTATCT CCCCACATCT TTACCAACTG TTATATTGTT AGACTTTGAT 240 TTCTGTCAAC CTTGTAGTAT AAAATGGTAT CATTTTAATT TTCAGTCCCC TGATTATTAC 300 TGAAGTTGGC TATTTTCTTA TGATTGTGGA TATATTTTTA GGTTTTTCCT TTTGTGAACT 360 GCCTGTTCAC ATCATTTGCC CACTTTTCTG CTGGGCTGGT TGTCTTTTTC TTACTGAGCT 420 GTAATAAATC TTTATGTATT CTAGGCATGA ATCCATTCTC TGTTATACCC ATGGCAGACG 480 CTTGGGAGGA TGTTTAGCAA GTTATAGGAA GAGGAAGGGG AAGGAGTTGA GAGGGAATGA 540 CAAGTTGAAG AAGGAAGGAT GAGAATAAAA GGTGGGGCGA GTCCGGGAAC AAGGCTGCGA 600 GGCTCGGGTG AAAGACTGGC CTTGAACTAG ATGAAGAACA CTTCCCCTGA GACCAGAGTG 660 CCTAAGAGTT CTGGGACAGT CTCAGTTGTA AAACAGCCAG TGCTTGGCCA CAGGTGTCAC 720 CCAATACACT GACTCAGCCA GGGCCTGGGA TGACTAAGAG CTTTTTCAAT GTGACTCATC 780 AAGGCTGACA AGCACAGGCA TCACGTTCCA GAACGCACAA CCAAAAGGGC AAAGCAACAG 840 TCCAGGCAGG TCAGCCTGTA GAGACAAGAC TTCCTACTGA CATCCAAGCT ACTCGTTTGC 900 CACAGCTGCT CCAAGGATGG CAATAATGAG TGCGAGCTGC ATCAGAGATG AGAGATTGAA 960 CTTTAAGAAA AATGTCGCCG GGCGCGGTGG CTCACGCCTG TAGTCCCAGC ACTTTGGGAG 1020 GCCAAGGTGG GTGGATCATG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA GATGGTGAAA 1080
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