| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108934029-108934519 | Common:8; Rare:194; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013438-109013760 | Common:2; Rare:111 | ||||
| chr9:109119490-109119545 | Rare:18 | ||||
| chr9:109498244-109498456 | Rare:69 | ||||
| chr9:110256431-110256725 | Common:5; Rare:106 | ||||
| chr9:110337854-110337995 | Rare:21 | ||||
| chr9:111038185-111038383 | Common:2; Rare:60 | ||||
| chr9:111371780-111371970 | Common:1; Rare:34 | ||||
| chr9:111484133-111484440 | Common:1; Rare:143 | ||||
| chr9:111525006-111525237 | Common:5; Rare:74 | ||||
| chr9:111599642-111599788 | Common:1; Rare:34 | ||||
| chr9:111599791-111599959 | Common:1; Rare:49 | ||||
| chr9:111631122-111631642 | Common:2; Rare:146 | ||||
| chr9:111661481-111661688 | Common:3; Rare:58 | ||||
| chr9:111758796-111759089 | Common:1; Rare:59 |