| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68631578-68632007 | Common:2; Rare:76 | ||||
| chr15:68817542-68817904 | Common:3; Rare:110 | ||||
| chr15:68820754-68821090 | Rare:103 | ||||
| chr15:69160342-69160635 | Common:3; Rare:87 | ||||
| chr15:69452672-69452848 | Common:3; Rare:79 | ||||
| chr15:72118167-72118403 | Common:2; Rare:75 | ||||
| chr15:72231114-72231534 | Common:3; Rare:136 | ||||
| chr15:72375957-72376144 | Common:3; Rare:75; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474210-72474316 | Rare:34 | ||||
| chr15:72686135-72686220 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633354-73633576 | Common:2; Rare:70 | ||||
| chr15:73994587-73994761 | Rare:34 | ||||
| chr15:74461107-74461314 | Rare:64 | ||||
| chr15:74540966-74541247 | Common:3; Rare:96 | ||||
| chr15:74598319-74598498 | Rare:77 |