| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151885-36152161 | Rare:84 | ||||
| chr5:36606447-36606619 | Rare:31 | ||||
| chr5:36876639-36876853 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:39074346-39074522 | Common:1; Rare:83 | ||||
| chr5:39425194-39425313 | Rare:25 | ||||
| chr5:40798152-40798348 | Rare:77 | ||||
| chr5:40835171-40835396 | Common:2; Rare:90 | ||||
| chr5:43121396-43121618 | Common:1; Rare:86 | ||||
| chr5:43483837-43483955 | Common:1; Rare:42 | ||||
| chr5:43603086-43603233 | Rare:36 | ||||
| chr5:44808787-44808955 | Common:1; Rare:53 | ||||
| chr5:53109725-53109885 | Common:1; Rare:79; Clinvar:2 | ||||
| chr5:54310524-54310711 | Rare:59 | ||||
| chr5:55307651-55308055 | Common:5; Rare:144 | ||||
| chr5:55994893-55995134 | Rare:86 |