Tag | Content |
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EnhancerAtlas ID | HS098-36109 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr21:45187650-45188600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr21:45188037-45188048 | CCACACCCTGT | + | 6.14 | NFE2L1 | MA0089.2 | chr21:45188220-45188235 | GCATGACTCAGCAGC | + | 6.64 | Nfe2l2 | MA0150.2 | chr21:45188218-45188233 | AGGCATGACTCAGCA | + | 7.3 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_00247 | chr21:45183479-45189887 | Adipose_Nuclei | SE_24314 | chr21:45186639-45188997 | Colon_Crypt_2 | SE_25151 | chr21:45186623-45188998 | Colon_Crypt_3 | SE_26733 | chr21:45186655-45189697 | Esophagus | SE_56219 | chr21:45187341-45193718 | u87 | SE_57364 | chr21:45187707-45188755 | VACO_503 | SE_65700 | chr21:45186464-45188577 | Pancreatic_islets | SE_67817 | chr21:45187341-45193718 | u87 |
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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 |
GH21I043767 | chr21 | 45186961 | 45189345 |
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Enhancer Sequence | CCCTCCCTGA GTGGGAGTTG CGAGTCCTTT GCCTTCTTCC CCCGTCTCCG GCTTGTAGCC 60 ACAAAATGTG CTGCCCTGGG CCCTGCCTCA GGTTTCCCTA CGGAAACGGC ACAGGCCACG 120 CTGCCTCCCC TGCTGGCACC CTAGTCTCTG ATGGAGACCG TGGCCTCTCC ACCCAGAAAG 180 TGGGCCAGGC CTCACCATCC CTGAGCTCTG TCTGCCTACG TCTCTGGCTG CCACTGACCC 240 CACCAGCATC TTGGCCTCTC GACACACCCC CTCCGCCCTG ACTCTGTGTC ATACCCAGGC 300 CTCACGACAC ACTCCTGGGC AAGGCTGCGT CGGCAGCGCC CTGGCCAGGG CTGTGGTCGG 360 GCCATGGAGG GGGCCCCCTG GCTGAGACCA CACCCTGTAC CCCCAAAAGA GGTCATCCTG 420 CCCGTGCCAG AAACCCCGTC AGGGACATGT GCACCCCTGG AGTGTGGGCG CAGAGGCCGG 480 CCACATTTAG CCAGTTGTAC ATTCATTCAG GCTGCAATTC TTTCTTATCC CTGGGCTCAG 540 GGCCGCACCC AGACACACGA GGCCGGGCAG GCATGACTCA GCAGCCCTTA GGATCTGCGT 600 CCTGTGATTT TCTCAAGGAG CACAAAGGTG AGCGTAGCCA TGGGGGAGAA TAGGGAAGGA 660 AGAAGGGCCA ACAGTGGCCG AGTCAGCTCT GCTTAGTCTG AACTGCCCCT CCCATTGCTC 720 CCAGGCCGGG CAGCAGCCTC TTGAGCAGCC CCGAGCCCCG CTCTTGTCCT TCCAGCCGGC 780 TCTCAGGGGC TCACCCCCTC CCCACCCCCA CAGTCAGCCT TGCGGTCAGC TTTCTCTAAA 840 GGCAGCTCCG CACACGTAGC TCTCCCTGCC CCACGTTGTC CACAGCGCTC CCTGCCCCCA 900 GATCCCAGTG TCCCCACCAC AGCTCCGCAC CGCTCCTTGA TCTGGGCCTG 950
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