Tag | Content |
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EnhancerAtlas ID | HS053-13403 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr15:41157740-41158860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLTF | MA0109.1 | chr15:41158655-41158665 | ATATAAGGTT | - | 6.02 | IRF1 | MA0050.2 | chr15:41158028-41158049 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | Nr2f6(var.2) | MA0728.1 | chr15:41157804-41157819 | GAGGTCAAGAGTTCG | + | 6.24 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_24292 | chr15:41158050-41158692 | Colon_Crypt_2 | SE_24964 | chr15:41158093-41158677 | Colon_Crypt_3 | SE_32137 | chr15:41157989-41158665 | Gastric | SE_47746 | chr15:41158069-41158751 | Pancreas | SE_65561 | chr15:41157793-41158886 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I040865 | chr15 | 41158017 | 41158663 |
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Enhancer Sequence | CCGGGAACAG TGGCTCACAT CTGTAATCCC TGCATTTTGG GAGGCCGAGG TGGATGGATC 60 ACCTGAGGTC AAGAGTTCGA GACCAGCCTG GCCAACATGG CAAAACCCCA TCTCTACTAA 120 AAATACAAAA ATTAGCCAGG CGTGGTGGCA CATGCCTGTA ATCCCAGCTA CTCAGGAAGA 180 TGAGGCAGGA GAATTGCTTG AACCCGGGGG ACAGAGGTTG CAGTGAGCCG AGATCACACC 240 ATTGCACTCC AGCCTGGGCA ACAGAGCGAG ACTTCGTCCC CCCCGCAAAA AAAAAAAGAA 300 AAAGAAAAAA AAAAGCCGCT GTCTGGGCCA TCTTGGAGTT CAGTTGTAAG GATGTATTAG 360 AGCGGAGGAT GGGAGGCAGC CTCCGCATTA CTGCATGCAG AGGCAGTAGT GCCCAGGTCC 420 AGGAAGTTAC TCCCTGCTCT TGCCACAGGG TGACTAATGT GGCCCCTCTG CTGAATTCTG 480 CTCACTGGGG ATCTGGCCCA GGCCCAAGGA GGGTGCTGGG AACAGGGTTT CCTGGCAGCT 540 GAAACACAGT GGGCAGGTCT GACCTGTGAG AACCGCAGTT ACTGCCTGAG GCCTGGGCTG 600 GTTACAGAAG GGGCTGGTGC TCCTGACGCA GTCTGCTCTC GGTCTCTCTG TAGCTCGTTC 660 CCAGGAGAAT GGGGAGCTCA GGGAAGGTGC GTCACCTCTG CCCTGGGCAC GACTCTGCTC 720 CCAGGGAGAA AGCAAGGCCA CAGCTCCTTC AGGTGTGCAC ACACTCACAC ACCAGCCCAG 780 TCCCAGCGTG CACACCCAGC ACAAACATGC ACACACAGAT CCACACAGAG ATGAGCATAG 840 GTACATACAG ATGCAGACAC ACTGCCCCAA GAAATGAGGT CCAGCCTAGC TGTATACACA 900 CAGGCATAGA TACACATATA AGGTTCTGTA TAATACACAC TTTTTTTTTT TTGAGATGGA 960 GTCTTGCTCT ATCGCCTAGG CTGAAGTGCA GTGGCGAAAT CTTGGCTCAC TGCAACCTCC 1020 GCCTCCTGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGCA 1080 TGCGCCACCA TGCTCAGCTA ATTTTTGTAT TTTTAGTAGA 1120
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