| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69414208-69414356 | Rare:40 | ||||
| chr15:69452688-69453047 | Common:5; Rare:149 | ||||
| chr15:70097837-70098092 | Common:1; Rare:59 | ||||
| chr15:70763373-70763694 | Common:2; Rare:101 | ||||
| chr15:70853944-70854302 | Rare:108 | ||||
| chr15:72118167-72118425 | Common:2; Rare:81 | ||||
| chr15:72230200-72230498 | Rare:79 | ||||
| chr15:72231120-72231523 | Common:3; Rare:130 | ||||
| chr15:72375957-72376129 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474195-72474620 | Rare:152 | ||||
| chr15:72475156-72475219 | Common:1; Rare:18 | ||||
| chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783469-72783535 | Rare:20 | ||||
| chr15:72783696-72783881 | Common:2; Rare:80 | ||||
| chr15:73633188-73633595 | Common:2; Rare:162 |