Tag | Content |
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EnhancerAtlas ID | HS065-01335 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr12:121351710-121352920 |
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) |
HES2 | MA0616.2 | chr12:121352016-121352026 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr12:121352016-121352026 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr12:121351934-121351949 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27043 | chr12:121352024-121353293 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I120914 | chr12 | 121352192 | 121353043 |
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Enhancer Sequence | TCGTTCCATT TATTTCCATG TCCACCCTCT TTTGTTGTTC TTATTATATA AATGACATCT 60 GTTATAAACC CCACAATACA ATGTCATAAC TTTAGCTCTT AAATAGCCAC ATCTGTCAGT 120 GTGCCTATAT GATTAAAAAA AAAAAAAAAA AAAAAGGAAG GCCCAGGTAC GGTGGCTCAC 180 ACCTGTAATC CCAGCACTTT GGGAGGCCCA GGCGGGTGGA TCACGAGGTC AGGAGTTCAA 240 GACCAGCCTG ACCAACATGG TGAAACCCCA TCTCTACTAA TAATAGAAAA ATTAGCTGGG 300 CATGGTGGCA CGTGCCTGTA ATCCTAGCTA CTCAGGAGGC TGAGGCAGGA GAATTGCTTG 360 AACCGGGACC CGGGAGGTGG AGGTAGCAGT GAGCCAAGAT CGCACCACTG CACTCCAGCC 420 TGGGTCCAGC CTGGGCTACA GAGCAAGACT CTGTCTCAAA AAAAAAAAAA AAAAAAAAAA 480 AAGGGACGCA ACCACGGCGG AAGAACAACT GCCAGTCTAA CTGTGCGTGA AGGCTGGCAG 540 TGATGGGGCC GAGACTGGGA ACCGCCCCTT CTCCCTGAGA CTGTTCATAG TGCTGTGGGT 600 CACAGGAGTC ACCTTCAACG TTACCACCAT TGACACCAAG AGACAGACTG AGAGAGTGCA 660 GAAGCTGTGC CCAGGAGGGC AGCTCCCATT CCTGCTGCAT GGCACTGAAG TGCACACAGA 720 CACCAACAAG ATGGTGGAAT TTCTGGAGGC AGTACTGTGC CCTCCGAGAT ACCCCAAGCT 780 GGCAGCTCTG AACCCTGAGT CCAACACAGC TGGGCTGGAC ATATTTGCCA AATTTTCTGC 840 CTACATCAAG AATTCAAACC CAGCACTCAA TGATAATCTG CAGAAGGGAC TCCTGGAAGC 900 CCTGAAGGTT TTAGACAATT ACTTAACATC CCCCCTCCCA AAAGAAGTAG ATGAAACCAG 960 TGCTGAAGAT GAGGGCATCT CGCAGAGGAA GTTTCTGAAT GGCAATGAGC TCACCCTGGC 1020 TGACTGCAAC CTGTTGCCAA AGCTACACAT AGTACAGGTG GTGTGTAAGA AGTACCGGGG 1080 ATTTAACATC CCTGAGGCCT TCCCGGGAAC GCGTCAGCAC TTGAGCAATG CTTATGCATG 1140 GGAAGAACCC GTCTCCACCT GCCCAGATGA TGAAGAGATC CAGCTCGCCT ATGAGCAAGG 1200 GGCCAATGCC 1210
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