| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44729306-44729528 | Common:1; Rare:46 | ||||
| chr15:45023048-45023241 | Common:3; Rare:51 | ||||
| chr15:45129910-45129996 | Rare:20 | ||||
| chr15:45200482-45200656 | Common:1; Rare:51 | ||||
| chr15:45201095-45201150 | Common:1; Rare:25 | ||||
| chr15:45522568-45522682 | Rare:26 | ||||
| chr15:45587146-45587491 | Common:1; Rare:97; Clinvar:6; Clinvar (benign):2 | ||||
| chr15:45587554-45587822 | Common:2; Rare:84 | ||||
| chr15:45634929-45635106 | Rare:53 | ||||
| chr15:47717843-47718123 | Common:2; Rare:60 | ||||
| chr15:47718389-47718595 | Common:1; Rare:52 | ||||
| chr15:48331367-48331457 | Rare:29 | ||||
| chr15:48645668-48645913 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr15:48878007-48878329 | Rare:122 | ||||
| chr15:49155528-49155895 | Common:4; Rare:119 |