| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92115346-92115513 | Common:1; Rare:51; Clinvar:1 | ||||
| chr9:92293654-92293844 | Common:3; Rare:68 | ||||
| chr9:92310610-92310857 | Common:1; Rare:57 | ||||
| chr9:92311212-92311360 | Rare:42 | ||||
| chr9:92325309-92325982 | Common:9; Rare:182 | ||||
| chr9:92670047-92670351 | Common:1; Rare:89 | ||||
| chr9:92877922-92877964 | Rare:11 | ||||
| chr9:93134228-93134356 | Common:2; Rare:45 | ||||
| chr9:93451430-93451702 | Common:3; Rare:73 | ||||
| chr9:93452297-93452372 | Rare:12 | ||||
| chr9:93453534-93453712 | Common:1; Rare:44 | ||||
| chr9:94259290-94259331 | Rare:13 | ||||
| chr9:94639416-94639563 | Common:1; Rare:41; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:94640176-94640311 | Common:1; Rare:30 | ||||
| chr9:95507418-95507485 | Rare:21 |