| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129753014-129753185 | Rare:44 | ||||
| chr9:129835217-129835487 | Common:2; Rare:109 | ||||
| chr9:130053840-130053935 | Common:1; Rare:33 | ||||
| chr9:130835142-130835402 | Common:8; Rare:84 | ||||
| chr9:131125417-131125651 | Common:2; Rare:111 | ||||
| chr9:132354938-132355186 | Common:3; Rare:78 | ||||
| chr9:132669930-132670039 | Common:1; Rare:52 | ||||
| chr9:132878308-132878426 | Common:1; Rare:44 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133348020-133348266 | Common:3; Rare:96 | ||||
| chr9:133356452-133356607 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr9:133375995-133376340 | Common:2; Rare:126 | ||||
| chr9:133524935-133525102 | Common:1; Rare:25 | ||||
| chr9:133738337-133738477 | Common:2; Rare:43 | ||||
| chr9:134371825-134371957 | Rare:38 |