| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104094487-104094589 | Common:2; Rare:31 | ||||
| chr9:104747608-104747757 | Rare:38 | ||||
| chr9:104928135-104928434 | Common:5; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105694372-105694566 | Common:3; Rare:76 | ||||
| chr9:106862973-106863186 | Rare:74 | ||||
| chr9:108934006-108934493 | Common:7; Rare:192; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:110048532-110048716 | Common:1; Rare:56 | ||||
| chr9:110256425-110256725 | Common:5; Rare:106 | ||||
| chr9:111525143-111525228 | Common:2; Rare:23 | ||||
| chr9:111599383-111599749 | Common:2; Rare:86 | ||||
| chr9:111661486-111661664 | Common:3; Rare:50 | ||||
| chr9:112379848-112380146 | Common:2; Rare:126 | ||||
| chr9:112718082-112718382 | Rare:64 | ||||
| chr9:113056657-113056836 | Common:1; Rare:64; Clinvar:1 | ||||
| chr9:113221262-113221619 | Rare:110 |