| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43371030-43371111 | Rare:18 | ||||
| chr15:43510624-43510954 | Rare:104 | ||||
| chr15:43517462-43517655 | Common:2; Rare:44 | ||||
| chr15:43824603-43824838 | Common:2; Rare:68 | ||||
| chr15:44536855-44537227 | Common:3; Rare:138 | ||||
| chr15:44711336-44711611 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45587324-45587461 | Rare:40; Clinvar:3 | ||||
| chr15:45634936-45635076 | Rare:39 | ||||
| chr15:48331383-48331465 | Rare:27 | ||||
| chr15:48878006-48878188 | Rare:72 | ||||
| chr15:49155565-49155832 | Common:2; Rare:93 | ||||
| chr15:49620806-49621093 | Common:6; Rare:113 | ||||
| chr15:50355074-50355504 | Common:3; Rare:170 | ||||
| chr15:50686721-50686914 | Common:4; Rare:81 | ||||
| chr15:50908601-50908729 | Common:1; Rare:43 |