Tag | Content |
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EnhancerAtlas ID | HS040-03751 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr10:1442120-1443490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr10:1443433-1443448 | CGGTGTGTGTGGTCT | - | 6.08 | HSF1 | MA0486.2 | chr10:1443062-1443075 | GAATGTTCTAGAA | - | 7.52 | Myog | MA0500.1 | chr10:1442375-1442386 | CTGCAGCTGTC | - | 6.62 | RREB1 | MA0073.1 | chr10:1442277-1442297 | TGGAATGGGGTGTGTGGTGG | - | 6.14 | Tcf12 | MA0521.1 | chr10:1442375-1442386 | CTGCAGCTGTC | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 1443298 | 1443391 | chr10 | 1442123 | 1442469 |
| Enhancer Sequence | TGTCACAGCC TGCATCTGGC CTGTGCTTGG GAGGTGCCAG TGCAGCCACA CTTTCCATTT 60 CTGTCTCTTA TTTTGGAGGT TGGCTTTGAG GGATGAGGAC AAACGTGAGG AGCGAGAATT 120 AGCAGGTTCA GATCAGGGGA AAAGCATGAA CCGCAGATGG AATGGGGTGT GTGGTGGGCA 180 GGGTTGGAGG CACCGCTGAG CGTGGGCAGA GAGGGGACAG GCTCCAGGGC TCTGCCTGCC 240 ACGTGGAGCC AGCACCTGCA GCTGTCCTGC GTCTGTCTCT CCTGCGTGGG TCGGCAGAGC 300 AGCGTGGGCT CCCCCAGGCC AATTCCACCG CAGGGCTGAG CCCTGGGCCT CCCTGAGTCC 360 GAGTCCGGGC AGCAGTTTTA CCATAAAAGG CGCATTTAGC AAACACACCT CAGGGCCTGG 420 ACTCTGTGTC ACAACTTCCT GAAGTGCACA GAGTGAGACA CATCGTGGTG AATCGCTGGC 480 CTCTCACTGC TCCCAGCAAC CAGCAAAGCA AGTCACGGCA GCACATGGAG ATGGATTTTC 540 TGGGAGAAAG GCAGCCGCAG TGCTCTCTAC TAGATGCCCT GAAAATCAAT CTGCAGCCCA 600 CTCCAGCCTG GTAAAATTAG ATCTAAAACT GGTTAATTTA GTTTCAGGAG TGTTTTCCCA 660 CCTGATGCCA GGCCTGAAGA CACCATGCAG TAAAGCACCC TGAGCTACTG CCAGCCCGTG 720 CTCCTCCTCT GGGTGGGGAC AACGCAGTGC TCCATGGCAC TGAGGGGCTG GTGCCCGGGA 780 CGAGATGGCA CTGCTCCCCT CCCCACCTGG TCACTGAGAG CCTCCTTTTC ATGCTGTTCT 840 TCTGCGTTCC ACACGGTTTG TAAAAAGGCG TGGCATGTGG ATGGTTTTAA TTTGCTTGAG 900 TGGGAGGGCT TATGGCTTTG GAGTTGGAGC CCTGGGACAG CTGAATGTTC TAGAAAGCAG 960 CTGTTTTGCA GCTAAGGCCT CAGCGACGGC TGAGTCAGGG AGGGCCGGGA ACGACCTCAA 1020 GGCAGGAGGG AAGAAGGCCT GAGAATCATC ACTGTCTCCA CCGGAACCTT AACCGCTGGG 1080 GCCCCTGACC ACGATTGGAA AACTGGAAAG AGCAAGCGCA GTATCAGAGA GTCCCAGGAC 1140 CCCTCGCCAG GGCCCCAGCC TGGCATGAAA TGGGATTACA TGCCTCCCAT TGTGTGTCCC 1200 GGCAGCCACA AACACCGTCA GGCCCAGCGT CACCCTCCCC ACCTCCCGGA TGAGAAGGAG 1260 CCTCCGGAGC AGCTGAGGGA CCCACTGTGG AGGCAGCCGG GTGGGGGACG GCCCGGTGTG 1320 TGTGGTCTGG TCGTGACTTT CCCACAAGGC ATCACCCATG GGAAGGAGGC 1370
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