| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95505886-95506195 | Common:1; Rare:106 | ||||
| chr9:95875449-95875709 | Common:1; Rare:88 | ||||
| chr9:95875961-95876037 | Common:4; Rare:37 | ||||
| chr9:96655289-96655424 | Rare:36 | ||||
| chr9:96778046-96778146 | Rare:32 | ||||
| chr9:97411927-97412177 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97501488-97501766 | Common:6; Rare:71 | ||||
| chr9:97633316-97633844 | Common:6; Rare:163 | ||||
| chr9:98255641-98255854 | Common:3; Rare:68 | ||||
| chr9:99221940-99222357 | Common:2; Rare:155; Clinvar:2 | ||||
| chr9:99821691-99821892 | Rare:65 | ||||
| chr9:99906570-99906694 | Rare:63 | ||||
| chr9:100098974-100099342 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352854-100353078 | Rare:79 | ||||
| chr9:101398511-101398905 | Common:1; Rare:140 |