Tag | Content |
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EnhancerAtlas ID | HS085-00425 | Organism | Homo sapiens | Tissue/cell | Heart | Coordinate | chr11:641940-643060 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr11:642867-642878 | GGGCAGGTGGG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGATGGCC TCAGCGGCTG CCTCCTCCAG GACACCTTCT CCGACTACCT GCTTCCCAGG 60 ACCAGCCTGT CCCAGTCACC CCCGGAACAG ACTGAGTCAC AGTGGATTCC TCTCAGACAC 120 CCGTGAGAGT GAAGGAGGGG CTCCCGCCAG CTTTGTCCCA GGACCCACAG CCCCACACGT 180 GCCTGACAGC GCTGGAGGCC ATGGGAGGTG CACATGCATC TGGGGGTCCT GGGGGTGCTG 240 ACAGCCCTGG GGCAGGGCGA CCTCTGACCA TCAGCCTCCC AGGCTTGGAA AGGAGGAGCT 300 GTGGAAACCT GGGATCCCAA CAGACGCGTG GTGCTTGGCT TCTGTTTTAC GGAAAGTTGG 360 GGAAGAGTAA GTGGCCCCCA CAATTCCAGG GAATACCCCC ACTCCATTCC TGCAGGGCCT 420 GGCGCAGGAA GCCAGGTGGC ATCACTGCTG GCGGGGGTCA CTGTGCCAGA GGGCTCCCAC 480 GGTGCCTCCC CCACCAGGCA GGGGTTCAGC TACTTCCTGC AGCTGTGCTC TCTGCAGAGA 540 TGCTGGTGTT CTCAGCTTTG GGGGATTATT CTTAAGAGGT GCAGGTCCTC AATTGCCTGC 600 CACCTTTATG TTGGTTAAAA CCCAAAGGAG CAGGCCCAGC CCTGCTGTCT CATGGAGGTC 660 AACCCACGGC CCGCCTGCCT GGACAGGGCA AGGCCAAGCA GGGCCTCTGA GATGCCTCCA 720 CCTTGCGGCA ATGGCAGACC CTGCTGGGTT GGATGAAAAG CCATTGTAGA GTCTCAGAGG 780 AAGGGCCAGG CGGGCTGAGG GTCAGAGGAA GGGCCAGGCG GGCTGAGGGT CACAGGAAGG 840 GCCAGGCGGG GTGAGGGTCA CAGGAAGGGC CAGGCGGGCT GAGGGTCACA GGAAGGGCCA 900 GGCGGGGTGA GGGACAGGCG GGGTGAGGGG CAGGTGGGGT GAGGTGCAGC ATCTGGAGCG 960 CGTCCTGCAG CAGCCCAGAC ACCTTTTCCA GCCTCCACTG CTCACTGGCA GCACCAACGG 1020 TGCAGCACCG GGCACGCCTG AGCAGGATGA TGAAACATCA GTGAGGGCTT GGCCTGGCTG 1080 GGCAGAGACT TTACTAAGTA AATAGGCCAG GGCGGTGGCT 1120
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