| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92293620-92293849 | Common:4; Rare:76 | ||||
| chr9:92325316-92325991 | Common:9; Rare:184 | ||||
| chr9:92670048-92670326 | Common:1; Rare:81 | ||||
| chr9:92877993-92878194 | Common:2; Rare:61 | ||||
| chr9:93453546-93453759 | Common:1; Rare:48 | ||||
| chr9:95516736-95517047 | Common:2; Rare:93; Clinvar (pathogenic):1 | ||||
| chr9:95875449-95875715 | Common:1; Rare:92 | ||||
| chr9:97633312-97633475 | Common:1; Rare:44 | ||||
| chr9:97633560-97633841 | Common:3; Rare:86 | ||||
| chr9:97922480-97922607 | Common:2; Rare:59 | ||||
| chr9:99221940-99222361 | Common:2; Rare:157; Clinvar:2 | ||||
| chr9:100098974-100099323 | Common:2; Rare:98; Clinvar:2 | ||||
| chr9:100352838-100353023 | Rare:62 | ||||
| chr9:101398591-101398898 | Common:1; Rare:99 | ||||
| chr9:104093985-104094350 | Common:3; Rare:89 |