| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98056486-98056773 | Common:1; Rare:92 | ||||
| chr9:98192611-98192859 | Common:6; Rare:68 | ||||
| chr9:98255637-98255890 | Common:3; Rare:82 | ||||
| chr9:98256130-98256179 | Rare:13 | ||||
| chr9:99104733-99105217 | Common:2; Rare:157; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99221884-99222355 | Common:2; Rare:189; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99821621-99822089 | Rare:137 | ||||
| chr9:99906575-99906717 | Rare:66 | ||||
| chr9:100098936-100099349 | Common:4; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352851-100353089 | Rare:86 | ||||
| chr9:100427034-100427384 | Common:7; Rare:127 | ||||
| chr9:100427746-100427849 | Rare:20 | ||||
| chr9:101028605-101029084 | Common:5; Rare:146 | ||||
| chr9:101398526-101398910 | Common:1; Rare:139 | ||||
| chr9:101487028-101487247 | Common:3; Rare:57 |