| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97852966-97853406 | Common:6; Rare:119 | ||||
| chr9:97922171-97922280 | Common:1; Rare:34 | ||||
| chr9:97922417-97922577 | Common:4; Rare:82 | ||||
| chr9:97983147-97983607 | Common:2; Rare:172 | ||||
| chr9:97984245-97984599 | Common:1; Rare:151 | ||||
| chr9:98056521-98056791 | Common:2; Rare:93 | ||||
| chr9:98119188-98119305 | Common:1; Rare:30 | ||||
| chr9:98192611-98192855 | Common:6; Rare:67 | ||||
| chr9:98255349-98255516 | Common:1; Rare:54 | ||||
| chr9:98255559-98256017 | Common:3; Rare:123 | ||||
| chr9:99221892-99222365 | Common:2; Rare:191; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:99821682-99822038 | Rare:99 | ||||
| chr9:99906570-99906717 | Rare:68 | ||||
| chr9:100098818-100099350 | Common:4; Rare:162; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352854-100353089 | Rare:85 |