Tag | Content |
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EnhancerAtlas ID | HS002-02780 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr12:131706640-131707870 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr12:131707730-131707751 | CTCCTCTCTGACCCCTCCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr12:131707741-131707762 | CCCCTCCTCCCTGCATCCTCC | - | 6.24 | ZNF263 | MA0528.1 | chr12:131707662-131707683 | GCCTCTCCTCCCTGCTCCTCC | - | 6.84 | ZNF263 | MA0528.1 | chr12:131707665-131707686 | TCTCCTCCCTGCTCCTCCTCC | - | 7.91 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34854 | chr12:131704520-131712029 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I131221 | chr12 | 131705668 | 131708234 |
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Enhancer Sequence | AGTCCTGGGG AGTCACACCC TACAAACCAT AAAATCTCAT GAAATGGGCT TTTCTATTAA 60 CCTGGTATAA TGGGGCTCAC CTTCCAGCCT GACTGTGGTA CGGCTCAGGT GACAGACAGC 120 AGACCCGTTC TCTTAACCCC AGCACCCCTT CTCCTGACTC CAAGACTTTA GACAAAGCTT 180 GGCTCTCTCA GCCAGCTGTG AGCTAAAAAG ATCCCGGAAA CCCACCGGTG ACTGGTAAGC 240 CCCGGCCTCC CGTGGTCCCG CCTTTGCGGG CTGAGCCGAC GTATCCCTTC CCTGCATGGA 300 TTCGTGATTG TGTCTGCAGG CCCTGTCTCT CTGCAATGCA TGAAATCAGC CGTAACCAGC 360 CCCTGGGGCA CTCTCAGGAA CTGCCCAGGC TGTGTTTCCT GGGCTGCGGG CACGCATACT 420 GGCTCAGAAT AACCTCTTTC AATATCTTGG TAGAATTTCG TTTTTCTATT GTCAGCCTGC 480 CAAGCCCTGT CTGCCTCAGT GCTGAATGTG AGTGTGTGAG TGCATGTGAG TGTAAGTACA 540 TAAATGGGTG TGTGAGTGTG TGTGCGTTCT GTAAGATGTG AGTATGTGTG CATGAGTGTG 600 TGCGTGTGCA TGTGTGTGTG CGTGTGCATG AGCATGTGTG TTTTAGTATG TGAGTGTGTG 660 TGTGTATCCT GCCGACTCAG CCACACCACC CCTGCTCTGC CCTGTAGAGA TAGCCTGAGG 720 CTCCTGGGCA GAAGATGGCC AGGTTCTGAC AACAGGAGTG GGTAGGAACC CGACGTGGGA 780 GGAGCCTGAG AGGAGGGCAC TCCCCAGCCC CCAGCTCCCA CCGCAGTGCC TCCATGTGGT 840 CCCAACCCTG GTGGCGCCTC TGCCCTACTG TCTGTCCCCA GCCAAGATGG ACCTTGCTGG 900 GTGGGAGGTG GGTGTCTCCC TGGTCCAGCA GTTGAGGGGA CTCCTGAGCC CTGCCCACTT 960 TCCCTCCCCT TGCCCCAGCC TGGGGGAGGT TACCGCGCTT CCCTGAGCCC CCGGCTCATG 1020 AGGCCTCTCC TCCCTGCTCC TCCTCCCTGC GCCCTTCAGC CTGCATCCTC CTCCCTGCCT 1080 ATCTTCCCTG CTCCTCTCTG ACCCCTCCTC CCTGCATCCT CCAACCTTGG CCCTCTTCCT 1140 TGTCCCCTCT TTCCAGGCCC CCTACCAGTC CTCGCCCCGG CTCTGTGTTT CCCGCTCTCC 1200 TGTGGGGTGG CGGGGCCAGG CCTCCCTTCT 1230
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