Tag | Content |
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EnhancerAtlas ID | HS108-26908 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:38158110-38159410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr22:38158723-38158738 | AGAGCTGAGTCATCT | - | 6.12 | Nr2f6 | MA0677.1 | chr22:38158507-38158521 | TGACCTTTGAGCTA | - | 6.11 | ZNF263 | MA0528.1 | chr22:38158626-38158647 | GGAGCAGGTGGGAGGGGAGAA | + | 6.69 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26673 | chr22:38158097-38159261 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr22 | 38158289 | 38158630 | chr22 | 38158689 | 38158821 | chr22 | 38158829 | 38159022 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I037761 | chr22 | 38157008 | 38159521 |
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Enhancer Sequence | ACTGTCACCC AGGCTACAGT GCAGTGGCAC AGAGGCTCAC TGCAGCCTCG AACTCTAGGG 60 CTCAAGCAGT CTTCCCACCT CAGCCTCCTG AGTAGGAACC ACAGGCTACA CCACCATGCC 120 TGGCTAATTA AAAAAATTTT TTTGTAGAGA CAAGGTCTCA CTATGTTCCC TGGGCTGGTC 180 TTGAACTCCT GGGCTCAAGT GCTTCTCTCA TGTTGGCCTC CCAAAGTGCT GGGGGTACAA 240 GTGTGACCAC TGCACTGGCC CACCTTTGTC CGTTTTACTC ATAGAGCCAG CTTTAGATTT 300 CCTTTAGATA AAGGCTCTGC CACTACAATG ACGTTTAAAA GGCACTGCTT TGGCTTCTCA 360 GCTTACTGGT GGCAAAACTG AGGCCCACAG AAGGGTGTGA CCTTTGAGCT ATAGGCAGAC 420 CTGTGTCTGG AGTTCAGGCG GTCTGGTCCC CAGGTGCCCC ATTGGGTGCA CCAAAGTCTG 480 TCAGTGTTTG GTCCCGTTAG GGTGGGATGG GCACGGGGAG CAGGTGGGAG GGGAGAAGGG 540 AATAACTGGG GAGCAGAGCT GAAGACCAGG CAGGTGGAGG AGTGACCCCA GATGCGGAAG 600 GCAGCAGAGA AGAAGAGCTG AGTCATCTGT ATCGCCCTCA GGCACGGGAG GAGGCGGATG 660 GAAATTCGGT GGACCTGGAG GAGTGACAGC TGGGAGGGAT TCCCCAGCTG GTATCTCGGG 720 CTGAGTGGGT GCCCTTCCTT CAGGGGTTGG GGGCTTGCTG CTGCACGACA GCTGTCGGGT 780 GGTCTGGGGC TTCACCCACT GGACATCTGG TAAAGAGAAC CTTTCCCCAC TATTGCAGTG 840 GGGACAGAGG CATTTCTTTA TCTACTTTGA TGTCCATGTC AAAGGTGGCA GCCAGGATCA 900 GGACACCTTG GGCCACTCAG GAAGGTAGGT GAGAGAGGCC CTAGGAGCCC CTGTTCGTCA 960 GCTGAGTCCC ACCTCCTGAT GTCAGCCCCT GCACCCCTGA GCTGCTGGGT CTGCCTGCCT 1020 GGTCTGGCCC TCTTCAGAAG AGCAGTGCCC ACCCCCACAT TGCTGGGCTC CCCACTGGTG 1080 GATGCTGGCG TACCGTCTCC CTCTGTGCAC AGGGTTCCCG TGCCCAGGGA GCCTCGGGGG 1140 CTGGTCCTGT GAGGCCTGCT TTACGGATGC CAAGACTGAA GCTCAGAGGG GGCGAGGGGT 1200 TTGTTCAGGT TCACTCCAAG GCGCAGCCAG GGTGAAGACC GCCTCTGAGG TCCAAAGTCA 1260 TGTTCTGTTG TCCTAAGCCA GGAGACACAT AGAGGGCAGG 1300
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