| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92293581-92293862 | Common:4; Rare:94 | ||||
| chr9:92325299-92325988 | Common:9; Rare:185 | ||||
| chr9:92670019-92670406 | Common:1; Rare:123 | ||||
| chr9:93452292-93452335 | Rare:5 | ||||
| chr9:93452336-93452351 | Rare:4 | ||||
| chr9:94640086-94640206 | Rare:22 | ||||
| chr9:95875441-95875661 | Rare:78 | ||||
| chr9:95875961-95876041 | Common:4; Rare:40 | ||||
| chr9:96655307-96655431 | Rare:29 | ||||
| chr9:97633279-97633848 | Common:6; Rare:177 | ||||
| chr9:97922471-97922566 | Common:3; Rare:47 | ||||
| chr9:97983121-97983470 | Common:1; Rare:129 | ||||
| chr9:98255593-98255909 | Common:3; Rare:96 | ||||
| chr9:99221906-99222355 | Common:2; Rare:175; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906601-99906690 | Rare:46 |