| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74173705-74173862 | Common:2; Rare:38 | ||||
| chr15:74461101-74461314 | Rare:66 | ||||
| chr15:74540966-74541290 | Common:4; Rare:115 | ||||
| chr15:74598322-74598553 | Common:2; Rare:102 | ||||
| chr15:74615560-74615907 | Common:4; Rare:109 | ||||
| chr15:74695941-74696051 | Rare:42 | ||||
| chr15:74843113-74843336 | Common:1; Rare:64 | ||||
| chr15:74873003-74873109 | Rare:23 | ||||
| chr15:74873281-74873456 | Common:5; Rare:58 | ||||
| chr15:74889964-74890089 | Rare:55; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74906777-74906880 | Common:1; Rare:46 | ||||
| chr15:74907247-74907478 | Rare:44 | ||||
| chr15:74937926-74938154 | Common:1; Rare:69 | ||||
| chr15:75201743-75201945 | Common:1; Rare:74 | ||||
| chr15:75335973-75336092 | Common:1; Rare:54 |