| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72473648-72474088 | Common:1; Rare:81 | ||||
| chr15:72474101-72474707 | Rare:202 | ||||
| chr15:72475120-72475181 | Rare:17 | ||||
| chr15:72475336-72475449 | Common:2; Rare:28 | ||||
| chr15:72685858-72685893 | Common:1; Rare:5 | ||||
| chr15:72686036-72686477 | Common:2; Rare:135; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72686529-72686745 | Common:2; Rare:48 | ||||
| chr15:72783478-72784234 | Common:4; Rare:244 | ||||
| chr15:72784277-72784558 | Common:4; Rare:43 | ||||
| chr15:73051790-73051958 | Common:1; Rare:47 | ||||
| chr15:73051964-73052393 | Common:3; Rare:122 | ||||
| chr15:73052614-73052680 | Rare:15 | ||||
| chr15:73632437-73632485 | Rare:13 | ||||
| chr15:73633202-73633722 | Common:4; Rare:187 | ||||
| chr15:73633803-73633819 | Rare:3 |