| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69414208-69414349 | Rare:39 | ||||
| chr15:70097883-70098092 | Common:1; Rare:48 | ||||
| chr15:70763328-70763422 | Rare:28 | ||||
| chr15:70854084-70854281 | Rare:62 | ||||
| chr15:70892381-70892823 | Common:1; Rare:97 | ||||
| chr15:72118167-72118422 | Common:2; Rare:79 | ||||
| chr15:72231102-72231516 | Common:3; Rare:129 | ||||
| chr15:72375968-72376137 | Common:1; Rare:67; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr15:73926294-73926471 | Rare:48 | ||||
| chr15:73994587-73994767 | Rare:36 | ||||
| chr15:74174239-74174593 | Common:3; Rare:69 | ||||
| chr15:74461107-74461314 | Rare:64 | ||||
| chr15:74540954-74541247 | Common:3; Rare:98 | ||||
| chr15:74615615-74615884 | Common:3; Rare:89 | ||||
| chr15:74843113-74843334 | Common:1; Rare:64 |