| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128675826-128675889 | Rare:7 | ||||
| chr9:128779845-128780117 | Common:2; Rare:85 | ||||
| chr9:128902867-128902971 | Rare:26 | ||||
| chr9:129003085-129003425 | Common:1; Rare:90 | ||||
| chr9:129006115-129006306 | Rare:66 | ||||
| chr9:129100521-129100915 | Common:4; Rare:126; Clinvar (pathogenic):1 | ||||
| chr9:129103012-129103251 | Common:1; Rare:61 | ||||
| chr9:129122845-129123127 | Common:4; Rare:83 | ||||
| chr9:129320812-129321013 | Rare:36 | ||||
| chr9:129352223-129352319 | Rare:44 | ||||
| chr9:129413770-129413981 | Common:3; Rare:97 | ||||
| chr9:129469475-129469599 | Common:2; Rare:23 | ||||
| chr9:129490975-129491090 | Rare:19 | ||||
| chr9:129496001-129496223 | Common:2; Rare:73 | ||||
| chr9:129621912-129622057 | Common:1; Rare:28 |