| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44288376-44288737 | Common:38; Rare:217 | ||||
| chr15:44427560-44427659 | Rare:30 | ||||
| chr15:44536564-44536631 | Rare:11 | ||||
| chr15:44536663-44537425 | Common:3; Rare:246 | ||||
| chr15:44663568-44663851 | Rare:140; Clinvar:9; Clinvar (benign):6 | ||||
| chr15:44711331-44711611 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728711-44729180 | Common:1; Rare:90 | ||||
| chr15:45023051-45023308 | Common:3; Rare:73 | ||||
| chr15:45201094-45201161 | Common:1; Rare:35 | ||||
| chr15:45402184-45402382 | Common:3; Rare:59 | ||||
| chr15:45587099-45587254 | Rare:26 | ||||
| chr15:45587271-45587470 | Common:1; Rare:58; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45634936-45635084 | Rare:41 | ||||
| chr15:48120867-48121180 | Rare:90 | ||||
| chr15:48331378-48331476 | Rare:31 |