Tag | Content |
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EnhancerAtlas ID | HS040-22494 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr20:45578180-45579800 |
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 | chr20:45579506-45579524 | AGAAGGAAGGCATGAAGC | + | 6.1 | KLF4 | MA0039.3 | chr20:45578281-45578292 | CCACACCCTCT | + | 6.02 | Klf1 | MA0493.1 | chr20:45578279-45578290 | AGCCACACCCT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27008 | chr20:45577467-45580047 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I046948 | chr20 | 45577468 | 45580047 |
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Enhancer Sequence | AGGATTTCAG TTGTTTTCTG ACTCTTGACT TGTTTTGTTC TTCTCCACGT TTTGGGTTTA 60 ACCTCAGCCT GCACATGGAG CTAGATGGTG GGGTAACTGA GCCACACCCT CTAAGGCACA 120 TAGTAGGTGC TCACCAAATA TTTATTGAAT GGATGGACTG CTCAAGATTG GCTTAAAAGC 180 TTGATACTTT TATGTAGCTG TTAGGTTGGT ATGCATTTTA AGATTTGTGT GTATCTGTCT 240 GTGTGTAGCC CAGAGGTTAA GAGTGGAAGC ACATTGCTTT GGTTGCAACC CTTGGCTGTG 300 CCACTTACCC ACTGTGTGAC TTTTGGCAAG GGTCCCAACC CCAGTTCTGC ACCTGCAACT 360 GCCCTATGAA GTAGGTAGTA TCATTTTGCA TCTATGATGC ACAAGGATAG CATGACACAA 420 AGAGGCTGAG GTGCTTGCAC AAGGTGATTT ATGGAGCTGG GTGTGCACCT TGGCATTCTG 480 GTTCCATAGC CTGTGTTTTT CTCCACTGTG CATGCAAAGT GCTCAACACA GTGCCTGGCA 540 CAGAGTAAGC TCCCAGTAAT CAAAAGAGCC ATCAATCCAG GCTCGTTTAA AGGTGGTGGT 600 GGACAGGGCA AGGGTTTCTC CCAGGATAAC ATGTAGTGAA GCATGGAGTT GAGTGATATA 660 AAAAATAATC ACTTTCCTAG AGTCTGGGAG AACTGAATTA TTATTTCCCA GCTGCCACTA 720 ATCTGCAGGG GGACCTTGCA GCGATGTTCC CCTCTCAGAC AGAGACTCAA TTTTCACAAC 780 CATAAAATAA TCTAAGGAGT CTCAAGTACC CTTCTAGCCC TGATATTCTA AGAGTCTGTG 840 ACTTGATGAT GCCTGTGAGT TTGGAGGTCT CATGGCTGGG CACTGAGTTT CCAAGATTGC 900 ACATGGTTTG GGGTGCTGGA GCTGTGGGGA AATCATGAGG AGTCACTCTG CAGCATCTGT 960 TCCCTGCTCC TCCTTCTGGG TGCTCCTCCA CCAAGGGGCA GGAAAGCCCA AACTCCCTTG 1020 CAGCTAGGTT TCTAGGAGTA ATGGAACATT AAGCAGGCAC ATGCGCTTCC TTGAAATTCA 1080 GAAGGCGGAG GTCGTACTCA AATTGCCTCT GCCGTGTTGG TTGTTTCTGT CACTGTGCAG 1140 AGTCTGGAGT AGTTTGGCTT GCTGCACAGC TTTAGCAGAG GCCCCAGCGA GCAGGCACTA 1200 GCTTTATGTG TGTTGAGAGG CATGGTGTCT TTGTGTGGGT TCCCAAGAAG CTGACCTCAA 1260 GATCAGGGCT CCAGTGCCAA TAGTTCATTT AAGAGGTGAC TCCAAGAAAC ACCAGAATGG 1320 GAATAAAGAA GGAAGGCATG AAGCGAAGGA AAGTAACAGA GGGTGTGTGA TCCAGCAGGT 1380 TACTCCCTGA GCATCTAAGG CTACACCCTG ATGGGAAAGG GCTTATAACA CGTGCCGCTG 1440 AGTAATCCCT CCTTAGGGGT GAGGGAGCTG GGGTCTTTAT ACCCCACATA TGCCAGAAAG 1500 AGCCTTCAGG TAAAACATTG CACTTGCTGC CGTTTGGAAG TTGGATGGTT TTCATGGAAA 1560 TGGTATTTGC CGAAGGGATT TAGGCAAGGT AGTGACAGCA TCAGCCACGC AGGGCACAGG 1620
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