Tag | Content |
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EnhancerAtlas ID | HS040-01899 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:67821490-67822450 |
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) |
Gata4 | MA0482.1 | chr1:67821902-67821913 | GAGAGATAAGA | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 67821585 | 67822244 | chr1 | 67821491 | 67822210 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I067355 | chr1 | 67820960 | 67822697 |
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Enhancer Sequence | TAGCAGACTT TTGAAGGAAA GAACATGCCC CAGCAAACAT CATGAGAGAG GAAATTCTAG 60 GTTGGTTCCT GGCAAGTGTG GTGACTCAGA GACAGAAGAA CCCTAGGCAA TGCCAAGTTG 120 ATTTACTTAG CTAATTCCAG AGAAAGTAGT GGTTAGAAAG GCTCTTTGGC TTTTTTACCT 180 CAATACTTGG CAAAGGATCT CGCAAACCAT AGTGTTCAAT AAATACTTGC TGAATGAGTA 240 AATTTTATTC TCAAAAAACA AAACAAAATA AAAAGCCCAC AGTATAACTG GGACATCAAA 300 TACCAAGGCA AGTGAAGACA AGGAACCATT GCTGGGAATT CCAGTTCCTG ACAAGATGTC 360 CAGTACACTG TCTACAGGCT CTACCACTAA ACCTGGCCCT GAAGCTGCTG CAGAGAGATA 420 AGATATGGAT GGCTGAGTTC CCCCTCTGGG GAATAGTGAT GAAGCGGGGA GGACCAAGGG 480 AGCTTTCTAC TTGTTCTCTT TGTTTTTTCC TCTTGTTATC CTGTTGTGAT CGCTGCCCAG 540 GAATCTCTAT GATGGGGTAG GAAATTCTGG GGAGCAGTGC AGAGTCACTG TCAAGGCAGC 600 CCTGGAACCT CACTGGGGAG GAGAGCTGGG AGCAAAGAGT GCCTGTGAGC TGGCTGACCC 660 TTCAGCATTT TTTTCCTGCC ACCCATCCCA TGGGCCTGGC AGTTTCAAAC AAGAATAATA 720 GCTCAATTCC CTCACGAAAA GCAGTGCCTA CCACAGAGGT ACTAGTTTGA TTCTGGAGGT 780 ACAAGTATGC CTAAGGGGTG CCTGGGGACA AAGAGCTCAG CTTGTATCAC TGCAGGGTCT 840 CTGGCCTGGA GCTTTCCAAG CTGAAAAGCC CTCCTCTCTA CCCTAAACAT ACATGGAGGA 900 CCATGAGCTA TAGCTGTACT TTGACTCCTC TCCCTATAAA AAAAGAAAAG CCAAGGTTGT 960
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