| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26956187-26956470 | Common:4; Rare:174 | ||||
| chr9:27573440-27573553 | Common:5; Rare:70 | ||||
| chr9:27573640-27574090 | Common:8; Rare:206; Clinvar:9; Clinvar (benign):2 | ||||
| chr9:32384471-32384732 | Common:2; Rare:183 | ||||
| chr9:32526077-32526601 | Common:8; Rare:197 | ||||
| chr9:32551950-32552390 | Common:4; Rare:214 | ||||
| chr9:32552537-32552637 | Common:1; Rare:18; Clinvar:2 | ||||
| chr9:32573029-32573243 | Common:5; Rare:135 | ||||
| chr9:33001512-33001758 | Common:3; Rare:125; Clinvar (benign):4 | ||||
| chr9:33025015-33025390 | Common:14; Rare:276 | ||||
| chr9:33076605-33076850 | Common:4; Rare:153 | ||||
| chr9:33166771-33166948 | Rare:94; Clinvar:6 | ||||
| chr9:33166890-33167595 | Common:2; Rare:428; Clinvar:13; Clinvar (benign):2 | ||||
| chr9:33239945-33240268 | Common:6; Rare:160 | ||||
| chr9:33263978-33264528 | Rare:337 |