| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93452307-93452323 | Rare:2 | ||||
| chr9:95055827-95056140 | Rare:63 | ||||
| chr9:95875453-95875698 | Common:1; Rare:80 | ||||
| chr9:95875972-95876041 | Common:4; Rare:33 | ||||
| chr9:97633316-97633829 | Common:6; Rare:159 | ||||
| chr9:97922471-97922560 | Common:3; Rare:46 | ||||
| chr9:98943580-98944026 | Common:5; Rare:140 | ||||
| chr9:99221940-99222329 | Common:2; Rare:139; Clinvar:2 | ||||
| chr9:99906591-99906684 | Rare:43 | ||||
| chr9:100098974-100099314 | Common:2; Rare:94; Clinvar:2 | ||||
| chr9:100352886-100353078 | Rare:62 | ||||
| chr9:101398588-101398910 | Common:1; Rare:102 | ||||
| chr9:104747609-104747763 | Rare:43 | ||||
| chr9:105558067-105558163 | Rare:28; Clinvar (benign):1 | ||||
| chr9:106862978-106863172 | Rare:66 |