| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43371021-43371127 | Rare:23 | ||||
| chr15:43510638-43510961 | Rare:102 | ||||
| chr15:43648949-43649021 | Rare:26 | ||||
| chr15:43746275-43746689 | Common:1; Rare:169 | ||||
| chr15:43776886-43777405 | Common:1; Rare:137 | ||||
| chr15:43792643-43793083 | Rare:128 | ||||
| chr15:43824556-43824805 | Common:2; Rare:74 | ||||
| chr15:44427269-44427692 | Common:1; Rare:108 | ||||
| chr15:44536855-44537425 | Common:3; Rare:204 | ||||
| chr15:44663532-44663845 | Rare:149; Clinvar:13; Clinvar (benign):6 | ||||
| chr15:44711291-44711627 | Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711825-44711982 | Rare:30 | ||||
| chr15:44712685-44712950 | Common:1; Rare:61 | ||||
| chr15:45114125-45114327 | Common:2; Rare:43 | ||||
| chr15:45200482-45200656 | Common:1; Rare:51 |