| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231123-72231466 | Common:3; Rare:109 | ||||
| chr15:72375957-72376129 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474178-72474325 | Rare:53 | ||||
| chr15:72686135-72686220 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:74461106-74461307 | Rare:63 | ||||
| chr15:74541088-74541288 | Common:4; Rare:78 | ||||
| chr15:74615594-74615891 | Common:4; Rare:98 | ||||
| chr15:74843106-74843318 | Common:1; Rare:64 | ||||
| chr15:74906789-74907070 | Rare:99 | ||||
| chr15:74938025-74938247 | Common:2; Rare:80 | ||||
| chr15:74995493-74995615 | Common:2; Rare:62 | ||||
| chr15:75335987-75336084 | Common:1; Rare:42 | ||||
| chr15:75347525-75347899 | Common:2; Rare:92 | ||||
| chr15:75368567-75368810 | Rare:72 | ||||
| chr15:75455799-75455957 | Rare:51 |