Tag | Content |
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EnhancerAtlas ID | HS040-10103 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr14:39672500-39673940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr14:39673210-39673222 | TGTCAGGGGGTG | + | 6.22 | NFE2L1 | MA0089.2 | chr14:39673311-39673326 | GCATGACTCAGCAGA | + | 7.23 | Nfe2l2 | MA0150.2 | chr14:39673309-39673324 | CTGCATGACTCAGCA | + | 7.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr14 | 39673628 | 39673859 | chr14 | 39673031 | 39673603 | chr14 | 39672861 | 39673002 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I039203 | chr14 | 39672488 | 39674045 |
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Enhancer Sequence | TGCGCCTGGC CTAGACTCTC TTTTTAAAGA TTAACTGGAG ATCATCATGG CGGATGGGAG 60 GCAGAACTAG ACTGCAGCTC TGACTCTGAT GGACAGAGCA GTGTGTGGAG GCTCACGTCA 120 TGAATTTTAG CTTCAGATCA ACTGCAATAA CAGACCACCA ATCCTGAGAG GACCCACAGA 180 CCCTCTGAGG GAAGCAGACT GCTCCTGCAG GACCTTGGAG ACACCCCAAA TATTGTGAGA 240 GCCCCAATTG CGGAAGTGGG AAAGCGAGAT CCTCCTCTCC CGAACACACA CCCCCTCTGG 300 AGAAACTGAA GGACTGTTTG CAGGAGAAGT TTTTGATCTT ACCTGGAGCT GATTCAATTT 360 AGACAGCCCA ACAAAATACA GGTGTAGAGG AAGCAGTAGG AAAGGCCCTG GGAACTTGCT 420 GGGTCCCCAG CAGGCCATTC CTGCCTGGCA CCACAGGGAT CTATCAGGAG AGTGGGCAGA 480 AGAGTGAGGG AAAACACCAC AGGGAGAAGG AAATCTCCAG CTGAACTTTG TGACAATTTG 540 AACCTGGTGA GAAGCCTCCT GGCCAGAACT CAGGGGAGGA TGCATATCAG TGTGCAGACT 600 CCACAGACTG GGGTAGAACT AAAGCCCTTT TATGTTGCAG CTGGGAGGAG GGTAGCCTGG 660 GGCAAGTTCT CAAGCCCAGC CCACCCACTG TCCAGAAACA GACTTGACGC TGTCAGGGGG 720 TGCATGGTGG GTGTGGGACC AGCTCTTTAG TTTGTGTGGG AGGTGGATGA GGCCTGTGAC 780 TGCCAGCTTT CCCCCACTTC CCTGACAACC TGCATGACTC AGCAGAGGCA TCTATAATCC 840 TCCTAGGTAC ACAACTCCAT TGACCTGGGA ACCTTACCCC ATCCCCCACA GCAGCCACAG 900 CAAGACCCGC CCAAGGATAG TCTGAGCTCA GACATGCCTA GCCCTGCCCC CACCTGATGG 960 GCCTTCCTTA TCCACTCTGG TAGCTGAAGA CAAAGGGCAT ATAATCTTGG GACTTCAAGG 1020 GCCCCACCCA CCACTGGTTC CTCTCCATAC TACCATAGTT GATGCTCTCT GGAAAGCATC 1080 ACCTCCCAGC AGGAGGCCAA CTAGCACAAA AATAGAGCAT TTAAACCACC AAAGCTAAGA 1140 ACCCTCACAG AGCCCATTGC GCTCCCCTGC CACCTCCACC AGAACAGGTG CTGGTATCCA 1200 TGTCTGAGAG ATCCATAGAC AGTTCACATC ACAGGGCTCT GTGCAGACAA CTCCCAGTAC 1260 CAGCCCAGAG CTGGGTAGAC GTGCTGGGTG GCTCGATCCA GAAGAAAGAC AACAATCACT 1320 GCAGTCTGGC TCACAGGAAG CCACATCCAT AGGAAAAGGG AAGACTCAAG GGACAAAAGA 1380 ATCTGAACAA CAGCCTTCAG CCTTAGACCC TCCCTCTGAT AGAGCCTATC CAAATGAGAA 1440
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