Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:43106018-43106156 | Rare:45 | ||||
chr15:43330543-43330700 | Rare:59 | ||||
chr15:43746287-43746467 | Common:1; Rare:70 | ||||
chr15:43826918-43827044 | Rare:57 | ||||
chr15:44288400-44288749 | Common:38; Rare:218 | ||||
chr15:44536855-44537192 | Common:1; Rare:118 | ||||
chr15:44711355-44711600 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr15:45587093-45587265 | Rare:32 | ||||
chr15:45587296-45587598 | Rare:107; Clinvar:7; Clinvar (benign):2 | ||||
chr15:45634929-45635079 | Rare:44 | ||||
chr15:48331367-48331476 | Rare:36 | ||||
chr15:49046371-49046675 | Common:2; Rare:104 | ||||
chr15:49155546-49155819 | Common:2; Rare:88 | ||||
chr15:49170128-49170260 | Rare:26 | ||||
chr15:49620794-49621099 | Common:6; Rare:123 |