| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:22008802-22009390 | Common:2; Rare:210 | ||||
| chr9:26892331-26892384 | Rare:20 | ||||
| chr9:26947058-26947274 | Common:1; Rare:85 | ||||
| chr9:26947444-26947610 | Common:1; Rare:44 | ||||
| chr9:27529693-27529819 | Common:3; Rare:36 | ||||
| chr9:27573429-27573526 | Common:5; Rare:50 | ||||
| chr9:32552432-32552676 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:32573046-32573211 | Common:2; Rare:62 | ||||
| chr9:33025071-33025382 | Common:7; Rare:127 | ||||
| chr9:33076605-33076831 | Common:2; Rare:76 | ||||
| chr9:33166856-33166975 | Rare:45 | ||||
| chr9:33167241-33167563 | Common:1; Rare:120; Clinvar:4 | ||||
| chr9:33239926-33240276 | Common:3; Rare:94 | ||||
| chr9:33264510-33265104 | Common:2; Rare:179 | ||||
| chr9:33290350-33290578 | Common:2; Rare:84 |