Tag | Content |
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EnhancerAtlas ID | HS040-01617 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:47076940-47078140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:47078010-47078023 | TTCTGGAAGGTTC | + | 6.19 | RREB1 | MA0073.1 | chr1:47077911-47077931 | CACCCAACCACCAACTCCCT | + | 6.44 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGCTTATAA AGGTGAAGCT GCTAGCCCAA GGCCACATAA GTATTAATCA GTGCAGAATG 60 GAGACTGGAT TCAGACCCTC TTTGCAGTGC ACTGCAGCGA CCCTCACAGA TATTGGGACC 120 CATGAAAAAG GCCCCGCTTC TGCATAGTCC CCCATGCTCA AGGCAGAGAT CTTGGTGGCT 180 TATGCCCTCT TCTCTGTGTG GCAGTCACCC AGGGTTTTAG GCATCGATAC CTGGAGTCCC 240 ACAGGCCCAG GGAGGTATGG CCAGCAGGGA CTATGAATCT ACATTCAGGT CCACAGCTGG 300 CCCACCCGGC TCTGTAGACC CCCTCCTCTT CCTCACCATT CCCAGGTGGG GTCGAGCCTT 360 CCCTCCCTCT GAGCCCCTCC AGCCCAGCCC AGATTCCTCA GACATATCCT GCCCATGTAG 420 ACTTGGGGTC CTGGGCTCCC ACAGATCTGA GCCCCAGTTC GGAATTCCTC CCAGTTCAGT 480 GCACTTTCCC TCAGTAGCCT CAAGTTTCCT CCTATGTAAA ATGAAGGTGC TCCTTGTCGG 540 GCATGACAGT GCAAGAAACA GCAGGCCACT GGCTGGGGAG GAGCCGTGGG CATTGAATTG 600 TGACTCAGTG CCCAGCTTCC TTCAGCATTC AGACTTCTCC CCTCAGGGCT TGACCACCCT 660 GCCCCACCCA CCGCTGATCC ACACAGCCTC TGCAGAGATG AGCTCCAGGC CAGGTGGGGG 720 CTGGGCCCAG CTACAGGTGC GGCTGGTGTG ATGAACACAG TGTCATGCCT GCTCAGCTCC 780 TGGACCAACA ACCCCCTCCT GCTGCCCTCG GGTGGGTAAG CAGTGCCTGG GTGACATCAC 840 TCATCTCCCC TCCCTACCCT CACCCGCCCA GGCTGCCCAG CTGAGATAAG AAAAGGCCCC 900 ACAGCCTGTG CCTGGCAAGG GAAAATTCTG TCCTCAGAGC CCCAATCTGA GGTGATGATA 960 CCACCAGGGC CCACCCAACC ACCAACTCCC TCCTTTTCCT GAGGCCAGGA GTCAGAGGGA 1020 ACCCCGGGAG GCTGGAGGTC AAATCAGCTA TGAACACCTC GGGGCAACTG TTCTGGAAGG 1080 TTCTGAGAAT CACAGCATCT GTGGTCTTGC CAGAGTGGTC CTTGGTGGGA CCACTTATGC 1140 TTTAGAAAAG AAAAGCCCTC TGAGGTGGGT GGATCACCTG AGGTCAGGTG TTCGAGATCA 1200
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