Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:37100269-37100784 | Common:1; Rare:153 | ||||
chr15:37101281-37101411 | Common:23; Rare:58 | ||||
chr15:37101716-37101853 | Rare:45 | ||||
chr15:38252488-38252803 | Common:1; Rare:127 | ||||
chr15:39580813-39581135 | Common:2; Rare:93 | ||||
chr15:39592808-39593668 | Common:3; Rare:182; Clinvar (benign):1 | ||||
chr15:39782794-39782882 | Rare:23 | ||||
chr15:40038864-40039350 | Common:1; Rare:172 | ||||
chr15:40340232-40340461 | Common:2; Rare:44 | ||||
chr15:40564965-40565125 | Common:3; Rare:28 | ||||
chr15:40569201-40569374 | Common:3; Rare:46 | ||||
chr15:40695076-40695180 | Rare:27 | ||||
chr15:40764009-40764105 | Rare:23 | ||||
chr15:40806909-40807119 | Common:2; Rare:42 | ||||
chr15:40807396-40807761 | Common:4; Rare:121 |