Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45201095-45201212 | Common:2; Rare:64 | ||||
chr15:45378481-45378678 | Common:4; Rare:55; Clinvar:1; Clinvar (benign):4 | ||||
chr15:45402211-45402360 | Common:2; Rare:43 | ||||
chr15:45587093-45587274 | Rare:33 | ||||
chr15:45587275-45587470 | Common:1; Rare:56; Clinvar:6; Clinvar (benign):1 | ||||
chr15:45587558-45587815 | Common:2; Rare:81 | ||||
chr15:45634923-45635101 | Rare:51 | ||||
chr15:48331022-48331153 | Common:3; Rare:33 | ||||
chr15:48331359-48331472 | Rare:39 | ||||
chr15:48645698-48645875 | Common:2; Rare:59; Clinvar (benign):1 | ||||
chr15:48877804-48878491 | Common:2; Rare:229 | ||||
chr15:49046357-49046643 | Common:2; Rare:100 | ||||
chr15:49155540-49155918 | Common:4; Rare:114 | ||||
chr15:49620769-49621093 | Common:6; Rare:124 | ||||
chr15:50119220-50119374 | Rare:24 |