Tag | Content |
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EnhancerAtlas ID | HS133-20798 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:46952940-46954450 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr21:46953927-46953942 | AGGCCAGGCTGACCC | - | 6.53 | SP1 | MA0079.4 | chr21:46953469-46953484 | GTGGCCCCGCCCACA | + | 6.34 | ZNF263 | MA0528.1 | chr21:46953060-46953081 | CCCACCCCCACCTCCTCCATC | - | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09718 | chr21:46951332-46956991 | CD14 | SE_31863 | chr21:46952733-46956163 | Gastric | SE_41708 | chr21:46952967-46953418 | LNCaP |
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Enhancer Sequence | CACTTGTCCC CAGAGCAAGG TCTTTAAGGC CAGACTCCAA CCCAGGAGCA GGGAGGGGGG 60 CAAACGCCCC TGTAGCCGCC CTGCACCCTC CCAGGAGGGG GAGCACAGGC TGTCAGCCTG 120 CCCACCCCCA CCTCCTCCAT CACATGTTAT GTGGGAACCC AGCTCCACAG CCTTGGCCAC 180 TGAGCTGCTG GTGGACACTC CAGGCCTGGC TTCCATGCCT GTGGCCTCAA CACACATCCA 240 CCTTCCATGG GAACGTGGAG CTGGGCACGG GGCTGGGGGT GCTACCTCCT ACAGGACAAG 300 GTCAGAGGAC ACTGCCCCAG ACTACTACAG GCAGGCACCA AACGTCCTCA GCTGTCTTGG 360 CAGGGGCCAG GGCTGCTGTG GGCACACCTG GGCACACCTG GGCACAGTCC AGAGGAAGAG 420 GCCCCACCCC TGTGAGGCCA AGCCGCTTGC CTTGCCCCTC CCTGGGGACT GATGTGGGAG 480 CCACCCTATG CTTGGAGCCT CCCCTGGGGC CCAGGTGCAT TTTCAGCAGG TGGCCCCGCC 540 CACAGGCCCC ACCAGACCCC ACCTCAGATC CACTGGAGGT TGGTACCAGA TGAGCCAGCA 600 GGGCCCTGCT GGACTCTGGG CCTCCAGCAG GCCCCACCCG ACTCAGGCCT GACCACCAGT 660 AACCCCACAG CCCCACTCGT GCTGCCCCAG GTGACCTCAG CCCCTGCCAG CCACACTTGG 720 CAGGACCAAA CCCTGGGTCA GCACGTGGGG TGCTGCGCCG AGCCACGCCG CCTCCCCGGG 780 GGCTCTCAGC CTCGTGTCTG GCACACCCAA GATGTGTGGC CCGATGTGCT CAGAGCCCGG 840 CCACCGGCTA CTGTGAACAG CTGGGCAATA GGACCCTGCA GCCAGGCCGG CATGCTGAGA 900 AGCTTCCCAG GGGCTCAGGG GAAGGCTGCC CAGAGACCCC ACCTCAGGGC ACCCTGAGGT 960 CGCACCCTGG AGCCTGCACC CTCATGGAGG CCAGGCTGAC CCAAAGGCTG TGGTCCCAGC 1020 AGCACCAGGC ACCCAAGGTC CCTCCGGCAC TCCGTCCTGC TCAGGACATT CCGGGACACT 1080 CTGAGGGCAG GTTATGTGCC AGGAGGCTGA GTGAGCCCGC CGGGTCACAG AGAGCCTCAG 1140 GGCCAGCCAT CGGCTTCTGC ACTGTGTTTA CAGCAATGTC CTGGGGACAT CAAACAGCCC 1200 CTCTGTGGGC AAGCTCTCCT GGCTGATGGC CTGCTCGACT GGGGGAGGCT CCTCCTCAGG 1260 GCCAGCCCAG GGAACCCCTG CAGATTCCGA AAGAAGCGGC TCAGAGGCAG GGGTCCTCCT 1320 AGGACCTCAG GGACCCCCGA CCCCCAGACA CAGGAGGCTG CGTGGGGGCA TGACAGCCCC 1380 AGCCCCTGGC CGGGGCACAG GTTCTGCCCA CAGCCCAGAG TCAAAATGGT AGACAGCCAG 1440 CAGAGAGGCT CTCCCCAGAC CCCACGGCTC TCTGGAAAAG GGCGGCCAGG GGTCCTAGAA 1500 GCCTCACCCA 1510
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