Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:42273394-42273487 | Rare:37 | ||||
chr15:42548725-42548868 | Common:2; Rare:78 | ||||
chr15:43330594-43330696 | Rare:35 | ||||
chr15:43493091-43493298 | Common:1; Rare:58 | ||||
chr15:43510688-43510961 | Rare:87 | ||||
chr15:43777114-43777403 | Rare:65 | ||||
chr15:44536672-44537192 | Common:1; Rare:158 | ||||
chr15:44711355-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr15:45129829-45130002 | Rare:38 | ||||
chr15:45378462-45378717 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):6 | ||||
chr15:45587322-45587487 | Rare:53; Clinvar:4; Clinvar (benign):1 | ||||
chr15:48331390-48331446 | Rare:19 | ||||
chr15:48645710-48645913 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr15:48877995-48878215 | Rare:91 | ||||
chr15:49155553-49155845 | Common:2; Rare:98 |