| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26947382-26947557 | Common:1; Rare:61 | ||||
| chr9:26956248-26956473 | Common:2; Rare:83 | ||||
| chr9:27573422-27573530 | Common:5; Rare:56 | ||||
| chr9:33001515-33001721 | Common:2; Rare:117; Clinvar (benign):4 | ||||
| chr9:33025065-33025383 | Common:7; Rare:130 | ||||
| chr9:33166779-33166989 | Rare:74; Clinvar:2 | ||||
| chr9:33167032-33167578 | Common:1; Rare:186; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:33264565-33264920 | Common:1; Rare:105 | ||||
| chr9:33264932-33265147 | Rare:66 | ||||
| chr9:33290369-33290570 | Common:2; Rare:78 | ||||
| chr9:33447408-33447762 | Common:4; Rare:100 | ||||
| chr9:33473837-33474139 | Common:4; Rare:93 | ||||
| chr9:33750577-33750721 | Rare:44 | ||||
| chr9:33817572-33817875 | Common:2; Rare:91 | ||||
| chr9:34048870-34048982 | Common:1; Rare:43 |