| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221865-99222361 | Common:5; Rare:384; Clinvar:6; Clinvar (benign):7 | ||||
| chr9:99821678-99822065 | Rare:191 | ||||
| chr9:99906549-99906739 | Rare:134 | ||||
| chr9:99907000-99907400 | Common:4; Rare:147 | ||||
| chr9:100098949-100099411 | Common:8; Rare:238; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:100352820-100353146 | Rare:210 | ||||
| chr9:100426440-100426800 | Common:5; Rare:69 | ||||
| chr9:100426820-100427340 | Common:9; Rare:224 | ||||
| chr9:101398585-101398918 | Common:2; Rare:209 | ||||
| chr9:101487005-101487233 | Common:5; Rare:108 | ||||
| chr9:101533728-101533921 | Rare:116 | ||||
| chr9:104093975-104094366 | Common:8; Rare:197 | ||||
| chr9:104094477-104094657 | Common:6; Rare:102 | ||||
| chr9:104747570-104747767 | Rare:94 | ||||
| chr9:104747810-104748090 | Common:7; Rare:157 |