Tag | Content |
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EnhancerAtlas ID | HS081-12996 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr22:42696550-42697710 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:42697687-42697705 | GGAAGGTGGGAAGCAATG | + | 6.3 | MYC | MA0147.3 | chr22:42697442-42697454 | AGGCACGTGGCC | - | 6.07 | SPI1 | MA0080.4 | chr22:42697165-42697179 | GAAATGCGGAAGTT | + | 6.68 | SPIB | MA0081.2 | chr22:42697167-42697179 | AATGCGGAAGTT | + | 6.27 | ZNF263 | MA0528.1 | chr22:42697672-42697693 | GGAGCAGCAAGGGAGGGAAGG | + | 6.82 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23330 | chr22:42695863-42698813 | Colon_Crypt_1 | SE_23842 | chr22:42696407-42698797 | Colon_Crypt_2 | SE_25072 | chr22:42695921-42698957 | Colon_Crypt_3 | SE_50938 | chr22:42695852-42698100 | Sigmoid_Colon | SE_56829 | chr22:42695891-42696837 | VACO_400 | SE_56829 | chr22:42697117-42697976 | VACO_400 | SE_65474 | chr22:42695910-42696986 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I042298 | chr22 | 42694880 | 42697851 |
|
Enhancer Sequence | GGACACACAC AGTGAGTGCT CAAGGGGTGC GGGCTAAGAC TTGGGGTCTC AGGACTCCCA 60 TGCCTGAAGC CTCCTGCGGT CAGCAGCCCA AGGGGCAGGG CTGTGGCTGC TGGGAAAGGG 120 AAGTATAGGG AGGTTAGTGG CAGGGGAGGG TCTCAGAAAA CCCCTCGTCC AGCCCAGGGC 180 CAACACACTC AGCCCCACTC ATCACCCTGA TGACTAACCC AGGCCTGCCT CTCTGCCTTT 240 GCCTCTGCTC AGCCCATCCT CCCTATCCAC TCCTGACATT CCCTCCTCCC CCTGCCAAGA 300 CCTGGGCAGC TTCCCCTCCC CCGAGCCCCA CCTGCAGAAT GCACCATGCA TTCAACCATT 360 CATTCTTCTG TTGCTCCCCA AGGCCCTGAG TCAGCCTTAA CCCCACCTTC AGAGGCCAGG 420 ACAGGGGAGG GTGTTTAGGA TAGAGAGGTG TGGCCTCCAA GGAGGAAGCA GCTACCTCTG 480 TAGGGTGGCG GTAGGGGAGT CTCCCCAAAG GAAGGTCCTA GGGCAGAGCA TGGCATCTGC 540 ACTTACCAGG GTGGAGGTGT AAATGGCTGC TGGAAGCCAG AGGCAAGGCT GGGAGGAGGT 600 GGATGTGGGG GTTCAGAAAT GCGGAAGTTT ATCTTGCGGG CACTAGGGAG CCGTTGGAGG 660 TGTGTAAGCA GGAGAGAGGT CGGCTCAGAT CTTCACTATG GGGCTGTCAG GACAAGGCGA 720 GGATGGAGTC ATTCATAGGT TCAACAAGTG TTTGCTGAGC ACTTACTCTG TGCCACGCCC 780 CAGGGAGACA GAGGAGAGCC AGACAGACAA GGCGTGCACC TTGGGGAGAC AGACGTGACC 840 ACACAACCAC CACCACAGGG TGAGGGGGCT ATGGTGGGGG CTGGACTGGG TAAGGCACGT 900 GGCCTGGTCC CTCCAAAGAG GAATCCACCT GCAAGGTGAG GACAGGAGGG GACACTGTTC 960 CCAGCCAAGG AGGTGGCATG CACACAGGCC CAGAGGTGGA GAAAGCAGGG CTTCCTAAGT 1020 CAAAGTGATT CGACAGGCGG AGGTGTCTGC AAGAGCCATG CCAAAGGTGA CAGAGCTCCC 1080 TGGCGTAGCT CCAGGGCAAT GGAAACCTTT GGGAGGGGTC TGGGAGCAGC AAGGGAGGGA 1140 AGGTGGGAAG CAATGTTTGC 1160
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