| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:5832956-5833211 | Common:8; Rare:204 | ||||
| chr9:6007915-6008079 | Rare:67 | ||||
| chr9:6015603-6015732 | Rare:111 | ||||
| chr9:6412968-6413361 | Common:5; Rare:259 | ||||
| chr9:6645635-6645975 | Common:5; Rare:212; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:6757082-6757491 | Common:6; Rare:198 | ||||
| chr9:6757440-6757755 | Common:4; Rare:177 | ||||
| chr9:6757770-6758346 | Common:11; Rare:332 | ||||
| chr9:12776010-12776423 | Common:4; Rare:242 | ||||
| chr9:14313830-14314360 | Common:1; Rare:242 | ||||
| chr9:14322290-14322870 | Common:10; Rare:337 | ||||
| chr9:14693246-14693390 | Common:2; Rare:125 | ||||
| chr9:15307138-15307445 | Common:4; Rare:271 | ||||
| chr9:15422578-15422904 | Common:2; Rare:284 | ||||
| chr9:15510150-15510520 | Common:4; Rare:293 |