Tag | Content |
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EnhancerAtlas ID | HS040-35877 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chrX:9756660-9758200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chrX:9757780-9757798 | GGAGGGAAGGAATGAAGC | + | 6.96 | FOXA1 | MA0148.4 | chrX:9757148-9757164 | CTTTATTTACATAGTC | - | 6.47 |
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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 |
GH0XI009788 | chrX | 9756400 | 9759051 |
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Enhancer Sequence | CTCTGGCCCC AGTGTTCAAG CCTGCTGCTC CCCTTCAGTC AGTGCCATCT GCTTGGGTCT 60 GGGATCTCCT GCAATGCCAT ATTGAATACC TTCGTCACAT CGGTTAGGTG AGGGTTTGCC 120 AGCCTTGGCA TTGGGGACTT TGTGAGCTGA ATCTCTTTGC TGTGGGGCTG CCCTGTGCTT 180 TGGAGGATGC TCAGCAGCCT CCCCAGCCTC TACCTGCTTG ATGCTACTGT CACCTCTCTC 240 CAGGTGTGAT GACAAAAATG TCTCCAGACA TTGCCAAATG TCCTCTGGGG GCAAAATTAG 300 CCTGGTTTTG AATCTCTTTT GTTAGATTAA CCATATATCA CCTTTGCTCT TAAAGGATTC 360 TTGCTCTTAA AACTTCTGTT TCTTTTTGAA TAGACTGGCC TTTAGGGTGG TGTGTTTAGA 420 GGCCTCTGGC ATTGCCAGTG TTTGCATGGA GAGCTGTTTT CCTCCCACGC GTTGGCCCTG 480 AGAATAGGCT TTATTTACAT AGTCAAACTC AAACAAATAC TTGCTTCATC TGCATTTTTT 540 GTAGCTGGAG AAAGGAAATT GAAGCAGGAA CTCCCAAGTG CTGTGTTTTA TGGGCATCCA 600 CAGTGGCTGT TCAGAATCAG GACTGACTAC TCTCTGGGTC TAGTTTGAAG CTAAAGGGAT 660 ACCAACTTCA GAGGAGTAGC ATTCTTGGAA TTTGGGGTGC ATGCATGAAG CCCAGCAGAA 720 CCTCCGCTGA CAGATGGCGA CAGGATTCAT CACTCCTCAG TACGTTTCTG CTGATTTCTG 780 CCTTGAAATT TTGCTACAGT TGGTGGAAAA AATGCACTCA AACCCATATT TCCATGCTGT 840 TGTTAGAGAG GGGGCAGGAA TAACATCCAT GCTGTAGGAA TCTATGTAAC GGAAGTAGAG 900 ATGGTGGATA TATGTGATCC TGGTGGGTTT TTTGCATGTT TCTGTTCCCA TCCATTCAAC 960 CAGTGGAAGT CTTCAGTGGG GGGAGGGGAG GGGACTGATT TCTAAAATGT CACTAGAGTG 1020 GCTTGAATTC CACAAAGCTG TTTGGGGGAT TCATGAGGAA GCGTTAAATA CACCAGCTGG 1080 GTGTCAGCAG CCCCCTGTGG CCTCAGGAAT GTTTGTTAAG GGAGGGAAGG AATGAAGCCC 1140 CAGCCTCTCC TGTTCACTAT TTCTTAGAGT CCGCTCCCTC CCCCAAAAAG AATGCCAGAA 1200 GCCTTAGCCC GAAGCTCCAA AGAAGACAGT AACTTGGGCC TGGCCTAGCC CCAAGGGCAG 1260 CTCCTTTGGG AACCCATTGA TTTTCGGGTT GCCATTGGGC ACCAGAGCTG TTGTGTGCGA 1320 CAAGACTGCT GTGGTCTGGG ACGCTTGGAG GTCCCCCCCA CCTGACTCAC CCACCCCAGG 1380 GCTTCAGACT CTGAGAACAT TTCTCTGGAT TGGAGACAGA GCTTTGAAAT GTCCTTTCCA 1440 GTGTGAATGC CAAAGACGGA ATCAGGGCAT ATTTTGGGGG GCGTGCAGCC AGGTGGCAAG 1500 TGTCTTATGT AAAGTGTTAG CTGAGTCCTT GATTGCAGAG 1540
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