Tag | Content |
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EnhancerAtlas ID | HS040-03794 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr10:3580180-3582340 |
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) |
FOXA1 | MA0148.4 | chr10:3580778-3580794 | CCTTAAGTAAATATTT | + | 6.05 | FOXC1 | MA0032.2 | chr10:3580781-3580792 | TAAGTAAATAT | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_44461 | chr10:3579873-3585720 | NHDF-Ad |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I003537 | chr10 | 3579994 | 3582614 |
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Enhancer Sequence | ACGCCAGCCA CCATTTAGCC CTTTACGTAT ATGGTTGGCT CATAAATACC CCTGAGAGGT 60 AGGATGGTTC CCACCCCATG ACAGATGAGG AAACTGAGGC ACAGGTGAGG CTGCCAGTTT 120 CCCCAACCAC TCAGCTGGGG TGTGGCAGGG CAGATGACAG AACCAGGGAC CACAAACCCT 180 AAAGGGCGGC AGCGGCAGCA GCAGCAGCAG CAGCCTCTGC ACGGGCACGG GTGGCGTTGG 240 TTTTGTGTGT CTGCTGTTTG TTAGGGGTCC AGCCTGTCTG TTGCTGCTGT CTGTGTGTCT 300 GTGTGTCTCA TGCGATGCAT CATTCATTGC ATGGGGACCC TGTTTTGAGG CCTATCCGAA 360 GTTTCATCCT GTTCCTAAGC TGCTCTAACC CGACTTCAGA GCTGTCTGCA TCTCAATCCC 420 ATGATCTCAC TCCAGAGGCA AAAACAAACC CTGTGAAGTG GGCAGACATT GCCCGTAACT 480 GCAAAGTGTA ACAATGTTGT TGTCATCATT ATCCAATAAC GCCAGAGCAA AGACATTGTT 540 TTTCACTTTT ATTATTATAC ATCAAAGATA TGGTATTTTC CATGTATGTT CATTTAGTCC 600 TTAAGTAAAT ATTTGTCGAT TACATCATTG GATCTTCACA GAAGTGGCTC CTGACTAAAC 660 AACACTGTAT TGTAAGAGAA ATGGCATCAT TTTTTAGCAT ATTTTCTCTT TAGAAAAGAA 720 GACAGAGATT TGAATTTGGG CGACACACAT AATAAAATGG ATGTTTTCTT TTTAACAACC 780 AAATCATACT CGAATTACAA AACCCTCCAG GCATTATCAG TTAATGCAAA CACAGGAGGA 840 AGATTTCTGC TCTCCGATTA CATAAAACGT CTCCCCATTC CCAAGATCCT GGAGCCTCTC 900 TCCCAGCGTC AGCTGTGGAC CGCGGGTTTT GCAGAACGGG AATTCAGGCA CTGTGATCTC 960 AGCCAGTGAG GAGGTCAGAT CAGGGCCCCA GGTTTGCCTG GTGGACCTTC CGAGTGGAAA 1020 GCAGCCAATG ATTTGTTACC ATGCAGGACA GCCGCCTCCG GGAACCCGTG TGTGGCCCGG 1080 GTGCCACGCA GCCTCGCGAC CCCTGCCTCT CTTCACTGGC TTGTTCTCTG CCTCAGTCAG 1140 AGCCAATGAC TTAGTGGCAT CACAATTTTC TCAAACTTGC CAGAACTTTC TGGAATGTAC 1200 TTAAAGAAAG CCATGACTCT GCCTCTTGTT AGCTGACATT CATTAGAGGC TTTGTGTCAG 1260 AGCTGGAAGC CATGAGTCAC ACTTGCTGAT ACAAGGGGAG ATCTCAGCAG GAGGAACGGG 1320 CCTCGTGGTG CCCGTGCGCT TCCTGGAATT GTGCTGTAAG TGAAATGAGA TGCTGGTGCC 1380 TGGGAGACCA GAGCTCAGCC CACATGGACT CCTCTGACAC TTCGTCTACA CTTAGAAACC 1440 TCCAAGCAGG CACAGGCCAG GCGCAGGTCA CTTTCTTCAG CCCCATCTCC CCAGGCAGCC 1500 CCAGAGGCGG CGGCAGTGGG CTCCCAACTT CATGAATCCG CTGGAGCACG GAGATGTGGC 1560 GTGAAAACAT GTCACACTCC TGGAGACGTG CATGAAGCCT CCTGGTGGCC TCAGAGTGTC 1620 TGGGGCCACC GGTCCTTTGA GATTTTAAGG AAAACAGTGT GTTTTCTGCT GTCTCCCCCT 1680 GACACAGCAC TCTGAAAATC AAGCCGGAGC ACCTGCAGAA CCTCAGCACT GTCCAGAGCA 1740 TCGTTGTGAG GGTCGGTTGC TGACCCAGGG CACGTCAGCC CCTGGAGGCC GAGTTACACT 1800 AACCTAGCCT CTGTTCCCTA CATTCCTTGG TGTGGACTCT GGAATGGACC ATGGAGAGAG 1860 AGGACATGAG AGCTGGAACT TTAATGCCCA TTCCTTCGGC TCTGGATGTG GGAAATACAG 1920 GTCATGCCGA GATAACACAC TTTTCACCAC AGGGGCGTTC ACAGGAAGGC CACACGCTTC 1980 ATGTCAAGGG TTAGACCAGA GGCTCAGGGC TGTGTATTCA CAGTAACGGC CAAGGAGGAA 2040 GGGATGGAGT TGATGCAACT GGAAACCCCC TTAGCAGTTG ACATTAGACC CTGTCTTGCA 2100 GAGGTGCTGA GGGACGAGCT GCCTTTGAAG CCTGGCGCAC GCATCTCCCA AGGCTGCGGC 2160
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