| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43648875-43649021 | Common:2; Rare:46 | ||||
| chr15:43746257-43746704 | Common:3; Rare:175 | ||||
| chr15:44536663-44537412 | Common:3; Rare:245 | ||||
| chr15:44711355-44711612 | Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711982 | Rare:24 | ||||
| chr15:45201063-45201153 | Common:2; Rare:37 | ||||
| chr15:45378481-45378634 | Common:3; Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr15:45587322-45587470 | Rare:44; Clinvar:4 | ||||
| chr15:45587521-45587796 | Common:1; Rare:94; Clinvar (benign):1 | ||||
| chr15:47718383-47718595 | Common:1; Rare:53 | ||||
| chr15:48331367-48331472 | Rare:34 | ||||
| chr15:48645704-48646014 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr15:48878004-48878524 | Common:1; Rare:190 | ||||
| chr15:49155538-49155845 | Common:2; Rare:102 | ||||
| chr15:49620747-49621093 | Common:7; Rare:128 |