| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128771833-128771980 | Rare:42 | ||||
| chr9:128881896-128882197 | Common:2; Rare:97 | ||||
| chr9:128921993-128922324 | Common:1; Rare:78 | ||||
| chr9:128947531-128947944 | Common:5; Rare:166; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:128999786-128999825 | Rare:11 | ||||
| chr9:129080987-129081134 | Common:2; Rare:43 | ||||
| chr9:129098250-129098577 | Rare:91 | ||||
| chr9:129108831-129108976 | Rare:25 | ||||
| chr9:129110499-129111029 | Common:6; Rare:155 | ||||
| chr9:129111224-129111624 | Common:3; Rare:109 | ||||
| chr9:129139204-129139447 | Common:2; Rare:56 | ||||
| chr9:129139897-129140145 | Rare:54 | ||||
| chr9:129141755-129142028 | Common:4; Rare:80 | ||||
| chr9:129626091-129626273 | Common:1; Rare:63 | ||||
| chr9:129626381-129626505 | Common:2; Rare:31 |