Tag | Content |
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EnhancerAtlas ID | HS116-20843 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr20:31446040-31447140 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr20:31446709-31446722 | GGGAACAGCTGCC | - | 6.24 | RARA(var.2) | MA0730.1 | chr20:31446868-31446885 | AGACCTCTGCCTGACCT | - | 6.27 |
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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: 2 | ID | Chromosome | Start | End |
GH20I032857 | chr20 | 31445561 | 31446891 | GH20I032859 | chr20 | 31446901 | 31447090 |
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Enhancer Sequence | GGAACAGACT TTTGTTTTTG TATGTTGGTG TTCTCTGAGT GGTGAAGGCC CAGGGAGAAT 60 GTTTTGTTTG GTGGTCACTT AGCATTTGAA AACATCCACT TCCTTGTGAC TTAGCTGGGT 120 ATCTTTTAAC ATCTGGAAGC CACGTCCCTG ATTGAAATCT CTGGAGACAA CTTACCTTTC 180 ACCAACTTGT CTGCCAAATT GCACCATGGA CCAAGATTGC AGTGGCTGCA TCAAGTCTAG 240 GCCTGCCCTG AAGTCTGGAT TTGTAAGTCC CCCATTTCAA ATGGGGCAGA AGGCAGAGGA 300 GCAGAGGAGC CACTGTGCCT TTCGCTGTCC TGGAGCCAGT TGGCCTTCTG GTTTTGGTGA 360 ACCCTGCTTT TATAAGAGGA CTCCCTGGCA TCTTCCAGTT TCCCGCTACT TGTTTTATGT 420 ATTATTTTAT GTCTGTGTTT GTCCTGGAGT GCTGTAACTC CTTTCACTGT CTGCTGTAAG 480 TTCAACTTCT TCAATAAAAG AAATGTTTCA AATTGGATGA AAAATGGTTC TGTGATTATG 540 GTTTGTGGGA CGGGTTCTGA TGCTTCATTT ATGTTCTTCA TACGGAATTC TGTCTCATTT 600 CCCTAGTTCT AAATATGACC AGCAGACCCA GAGTTCCATC TCGACTTCAT AAAGGAGCTG 660 TCTTGGACTG GGAACAGCTG CCAATGTCTT TGTTGAGATG GGAGTTGGAA AGTGTTAGCA 720 CTTTGCCAGA CTTTGCCAGC AAGATTAACT GAGGAGATCA AATTGAGTCA GGGTGAGTGA 780 GGGTTTTAGG TGAAAGTTGC TCTCCAAAAG ATTGGATACC TCTGCTGAAG ACCTCTGCCT 840 GACCTCCAAG GCTGGAGAGC AGCTCTTATC TGTGTCCTGG CTGGCTTTCA ATGCATGTAT 900 CCTTAAGTCA TCTGCCTCTA CAAATTCGTA CAAACCACTC GTTCCCCTCT CATCCCTAGC 960 ATGTTCCCCT AGTGGCTGCT CTGAATTCTC ACCCCTGTTC TGGATGGTAC TCTCCCACCT 1020 GCCTTGCCCT GCCCCTCTTC CGTCAGCTCC GGACAGGTCA ACTTTAGGGA ATAGATTGAG 1080 GCAGATGGAT GTGACTTCTG 1100
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