Tag | Content |
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EnhancerAtlas ID | HS002-06352 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr21:44802700-44803740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr21:44803035-44803046 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr21:44803035-44803045 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr21:44803032-44803047 | GTGGCCCCGCCCCCC | + | 6.4 | SP3 | MA0746.2 | chr21:44803034-44803047 | GGCCCCGCCCCCC | + | 6.11 | SP4 | MA0685.1 | chr21:44803032-44803049 | GTGGCCCCGCCCCCCCT | + | 6.58 | Stat4 | MA0518.1 | chr21:44802719-44802733 | CAGTTTCCCGGAAG | - | 6.15 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_11196 | chr21:44798231-44805256 | CD20 | SE_31895 | chr21:44802935-44803934 | Gastric | SE_58455 | chr21:44763901-44850830 | Ly1 | SE_62541 | chr21:44767678-44851140 | Tonsil | SE_65619 | chr21:44801680-44805042 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH21I043379 | chr21 | 44799286 | 44803990 | GH21I006154 | chr21 | 44802938 | 44803549 |
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Enhancer Sequence | CCCTGCAGGT GTGCAGGGGC AGTTTCCCGG AAGCCATTCC TGTTCTGGAC AGCTGTGAGG 60 TACCCATAAG TGACCATGAG CCATCTGCAC AGTCATCCCA TAACCCCAAC TAGATACAGT 120 TTGGGTATCT GTGCCCCCCA AACTGTGCCA ACAAGGGGAG GGTGCCTGGG GTGGGGAGAG 180 AGGCTGCCGG GTAGAGAGCG TCAGGTGGGA AACAGGACTG GGCTACACAC TTTTGTGGAG 240 TTTGCACCAC TCACACCACT CACACCAGCT GCCAGAACAC TTCCTGTCCA GGGCCCAGCG 300 CCTCTGGCAG GTGGGAGCCC CATTCAGTGA CCGTGGCCCC GCCCCCCCTC CCCCGAGCCT 360 CCAAAGAAAG GAGCCGTTGT TTATCCAGCA ACAAGCCGTG TGGATAGTGA GGATCCCGGG 420 AGGGGACAAG GAGCAACTGA ACACTGGCTC CATGGGACAA AGGCACCGGC TCTCAGTCTC 480 CAGAGTGTGG TCCCCTGGCT TGTTGAGAAA CCCCGCGGGA CTGGGGAGGG GGAAGGGGGC 540 AGGGGGCAGA GCAGGTGTGA CTAGGACCCA ATAGCCAGCG TATGTGTGGC TGGTGCAGTG 600 CTACTTCCGT CCCCCTCCTG AGCCCCCCTT GAATCAAATG GCACCGTCAC CCCTGCAGAG 660 CGCGAGAAGC CACCCGCCCG GGAGCTGCTA AACGTCATTA AGTCCCTACG GTGACGGTGA 720 CGCAGGCACT GAAAGCTCTG AGAAATAGGC CGGCAGAGGG AGGGAGGGAG GGATCCAGGA 780 TGCCAGGCCT TTGTGTCCCC GTCACGCCAG GCTCAGGGAC GTCGGGGACA TCGTCTGAGC 840 CAGGAAAGAA GGAGGCTGGG GGCTGGGCCC AGGGCAGGGG CCCTGTGTGT ATAGGAAGGG 900 AAGCCCCGGG CAGGGAGCCC AGCCCTCCGA ACGCAGCCTG CTAAGGGCAC CGGGAATTAA 960 GACGTGAAAG GCACACAGCA GAACGCGCGT GGGCCTCGAA AGGCTCCCTC GGAGCTCTTC 1020 ATGGGCTGGC CCCAGGAGTG 1040
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