Tag | Content |
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EnhancerAtlas ID | HS040-02135 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:110777650-110778930 |
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) |
JUND(var.2) | MA0492.1 | chr1:110778708-110778723 | GATGACCTCACTTTT | - | 6.05 | Sox3 | MA0514.1 | chr1:110778878-110778888 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65653 | chr1:110775910-110779459 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I110234 | chr1 | 110777486 | 110779509 |
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Enhancer Sequence | CCCTCCCTGC CCTGTTCCTG TCACTCTCAG ACTTTTCTCC ACAGACTTCT GAGATCTCCG 60 TGTCCAGCTG CACCAAGAAA GGACAAGAAC ACACCCGGGA GCTGTCTTGG GCAGTGTAGA 120 ACAGCAGGGT GAGGACGGAA TGGCCGAGGA GAGGGAAGAA GCCAGGGGAA GCCTGTTCCT 180 GAAGTGTAAG GAAAGATCGG GCTTGGAGCC TGGGCCAGCC GAGGCAAGGG GGTGGCAGGC 240 AGCCAGTGTC AATTAAAGAT AAAATTTCTC CTCCGGTAGT GGAGGGCAAA CAGTGGCTGT 300 GGCCCCCCTA GACAGGAGAA AGCCATTTGC AGCCAGGCTG GCCTTGGAAA AGCTTGGCCA 360 GGCGATAATG GGACGGGATG CGCTGCTGAC TCCATAATGA TATTACGCAT CAGGGCCCAC 420 GGCCAAAGTG GCTGTTTTTT CTGTAGATCG ATGTGGAACC ATTTCATGGT CAGGGGCTGA 480 GAACCCAGCC AGCAGCAGGG GTACTAGATG CCAGAGTGGT CCTGAGGGGA CTGAAGGGGT 540 GGCAACTGGG GTCCCCAGTG ACCGTTTCAG GCTGCTGGAA GAGGAGGGGG CAGTGTGCAG 600 GAGGGTGGAG GGGTGGACGA GAGAAGCAGC AGACTGCCCC TCCTCCCCAC CTCACAGAAA 660 CAGCAGGCCG TGCTGTCAAG GAAGAAAGGG CTCTGGCTTC CTCCTGTTCC CCAAAGCTGG 720 AGTCGAGCCC AAGGTAGGGA GCTGGTTAAA AGAACAGGAC ATTGTTTAAA AGAATAAGAC 780 AGACTTTTGA AGTCAGGCAG ACTTGGGTTT GAGTCCTGAC TCCATCACTT CCTTGTTGTG 840 TGACCCTGGG CAAGTTACTC AGCCTCTGTG AACGTCTATT TCCTCATCTT TTAAATGTAG 900 TATCTGCCTG AGGCCGTGTC TCTCTCATTG AGCCATGAGG AGAAATGAGT CGGCGCCTGT 960 AAAGCCTCGC GCACAGTGCC TAGCACATAA CCATTGCTAG AGGGAGAGGG GAGTATTTTG 1020 GGGCAACTCA CTCCAGTAAC AGATGACCAG TTTGGTTTGA TGACCTCACT TTTCAGTGAA 1080 TCAGCCTCAT TTCACTGAAG TCCTTAGTCC TTATCTCCTT GTGAAGGAAT AAGAGGGGAT 1140 GATTATACCT AACAGCGAAC ATTTATTGAG TGCTGGGCAG TACATTTCAT GCTTATAAAG 1200 ATGCATTCCA AGATTGATGT TATCCTTACC TTTGTTTTAC GAGGAGAAAA CCAACACAAC 1260 AATGTCAGGT CATTTCTCCA 1280
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