| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33264676-33265102 | Common:1; Rare:117 | ||||
| chr9:33817784-33817917 | Rare:27 | ||||
| chr9:34049175-34049315 | Common:1; Rare:34 | ||||
| chr9:34329186-34329594 | Rare:130 | ||||
| chr9:34637725-34638125 | Common:3; Rare:105 | ||||
| chr9:35072555-35072904 | Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35658018-35658376 | Common:6; Rare:230; Clinvar:15; Clinvar (benign):10; Clinvar (pathogenic):24 | ||||
| chr9:35685535-35685783 | Common:1; Rare:68; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689705-35690022 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35699043-35699406 | Rare:88 | ||||
| chr9:35731949-35732361 | Common:2; Rare:113 | ||||
| chr9:35732365-35732709 | Common:3; Rare:87 | ||||
| chr9:35749219-35749378 | Common:1; Rare:75 | ||||
| chr9:35814978-35815250 | Rare:71 | ||||
| chr9:36190653-36190989 | Common:1; Rare:107 |