| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95875459-95875741 | Common:1; Rare:103 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:96778055-96778156 | Rare:32 | ||||
| chr9:97039056-97039290 | Rare:89 | ||||
| chr9:97633271-97633848 | Common:6; Rare:177 | ||||
| chr9:97697293-97697409 | Common:1; Rare:73; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:97922171-97922324 | Common:1; Rare:56 | ||||
| chr9:97984466-97984600 | Common:1; Rare:68 | ||||
| chr9:98255598-98255843 | Common:3; Rare:75 | ||||
| chr9:98943394-98943597 | Rare:39 | ||||
| chr9:98943746-98944064 | Common:3; Rare:109 | ||||
| chr9:99221906-99222365 | Common:2; Rare:182; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99821682-99822038 | Rare:99 | ||||
| chr9:99906575-99906684 | Rare:54 | ||||
| chr9:100098972-100099323 | Common:3; Rare:98; Clinvar:2 |