Tag | Content |
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EnhancerAtlas ID | HS040-11681 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr15:59023750-59024660 |
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) |
GFI1 | MA0038.2 | chr15:59024546-59024558 | TGCAGTGATTGC | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH15I058731 | chr15 | 59023371 | 59025599 |
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Enhancer Sequence | CACGAAGTCG AGGCTGGGGT TAGCCGTATT CACACCACTG CACTCCAGCC TGAGTGAGAG 60 AGTGAGACCC TGTCTCAAAA AAATAAAAAA ATTAAAATTC AAGTATGAGA GGGCATTTTG 120 CAGTGAGGCT CAGAAGGCAA CAAGCACCCT GAGGTGACCC CACCCAAGGT AACTGGTATG 180 GAGTGGAGGA TGAACATGCA CCTTCCAAGC AGGGTGTTTC TTTAAGAGTG TCACAGGTGA 240 GAATTCCTAA GGCAGGTCAG AAAGCCCACC CCATGACATG TGCGGCCTGG TCTTGAAAGA 300 CGTTTTTCCA TCTAGCTGGA CAAGGGGAAC ATTCTCTGAA TAGCAACCAC ACACATGTGA 360 GTCATGGGGT GGAGACTTCT GGTTCACTGT AACCTAGACC AGATTCAGAG GCAGCAGACA 420 GAAATCTTCT AGAAGGAAAA GAGCCTGGTG TTTGTGAAGA TCTGCAGATC CTACATGTCA 480 AAGAAGGTTT TCACTAGCAG GAAGGGTGGA AAATACTTCT TGAATAGCTT TGAAGTTTTC 540 AAGCACCAGG CCCCTCCCAA TGGGGAAGAA GCCACACCAA AGTACTGAGA GTAGGGAGGC 600 CTTTCACACT GGACAAAGGG GCTGCAAGTG CAGTGATGTG GGAAAGCCTT CAACTGCAAA 660 GATAAACTTG TTCAGCAACA GAAAATCCAT GACGGAGTAA AGCCTTAGGA GTGTGGTGAA 720 TGTGGAGAAA ACCTTTAGTC ACAACTCCTA CTTTACAGTA CAAAGAAGAA TTCACAGCAA 780 AGAAATACCT TATAAATGCA GTGATTGCGG GAAATTATTT GGCTCCACCT CCAACCCTCA 840 TACTTTAAAG AGGTCATACA AAGAATGAGC TTAAAGCCAG GCATGGTGGC TCATGCCTGT 900 AATTCCAGCA 910
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