| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92293587-92293811 | Common:3; Rare:70 | ||||
| chr9:92325629-92325953 | Common:3; Rare:90 | ||||
| chr9:92670048-92670362 | Common:1; Rare:90 | ||||
| chr9:96655307-96655458 | Rare:36 | ||||
| chr9:97633312-97633475 | Common:1; Rare:44 | ||||
| chr9:97633497-97633848 | Common:4; Rare:115 | ||||
| chr9:99221916-99222365 | Common:2; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99906601-99906702 | Rare:50 | ||||
| chr9:100098974-100099317 | Common:2; Rare:95; Clinvar:2 | ||||
| chr9:100352860-100353071 | Rare:72 | ||||
| chr9:101398588-101398910 | Common:1; Rare:102 | ||||
| chr9:104093985-104094274 | Common:3; Rare:68 | ||||
| chr9:104747426-104747757 | Rare:82 | ||||
| chr9:105558086-105558170 | Rare:20; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862981-106863166 | Rare:64 |