| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111525082-111525237 | Common:5; Rare:55 | ||||
| chr9:111599367-111599507 | Common:2; Rare:36 | ||||
| chr9:111661484-111661703 | Common:3; Rare:61 | ||||
| chr9:111896633-111896813 | Common:3; Rare:72 | ||||
| chr9:111897317-111897565 | Common:3; Rare:60 | ||||
| chr9:112333469-112333959 | Common:1; Rare:145 | ||||
| chr9:112379759-112380192 | Common:4; Rare:161 | ||||
| chr9:112717997-112718160 | Common:2; Rare:40 | ||||
| chr9:113056657-113056893 | Common:1; Rare:77; Clinvar:1 | ||||
| chr9:113150641-113151036 | Common:5; Rare:93 | ||||
| chr9:113187856-113188181 | Common:5; Rare:60 | ||||
| chr9:113221214-113221649 | Common:1; Rare:138 | ||||
| chr9:113275354-113275734 | Common:5; Rare:122; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340433 | Common:3; Rare:50 | ||||
| chr9:113376896-113377093 | Common:7; Rare:62 |