| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72117944-72118671 | Common:6; Rare:227 | ||||
| chr15:72228792-72229159 | Common:2; Rare:61 | ||||
| chr15:72231069-72231580 | Common:5; Rare:165 | ||||
| chr15:72231584-72231755 | Common:1; Rare:37 | ||||
| chr15:72231795-72232027 | Common:2; Rare:46 | ||||
| chr15:72272457-72273018 | Common:3; Rare:145 | ||||
| chr15:72320137-72320397 | Common:1; Rare:83 | ||||
| chr15:72375618-72375779 | Rare:41; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr15:72375908-72376199 | Common:4; Rare:113; Clinvar:11; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72473645-72474025 | Common:1; Rare:65 | ||||
| chr15:72474108-72474417 | Rare:107 | ||||
| chr15:72475119-72475366 | Common:1; Rare:70 | ||||
| chr15:72685648-72685780 | Common:1; Rare:26 | ||||
| chr15:72685856-72685888 | Common:1; Rare:5 | ||||
| chr15:72685900-72686478 | Common:3; Rare:166; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 |