| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128787034-128787333 | Common:4; Rare:89 | ||||
| chr9:128881929-128882197 | Common:2; Rare:91 | ||||
| chr9:128921375-128921422 | Common:1; Rare:8 | ||||
| chr9:128921983-128922318 | Common:1; Rare:76 | ||||
| chr9:128947580-128947747 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:129036335-129036672 | Common:2; Rare:91 | ||||
| chr9:129080802-129081144 | Common:2; Rare:94 | ||||
| chr9:129110653-129110960 | Common:4; Rare:70 | ||||
| chr9:129111291-129111593 | Common:2; Rare:82 | ||||
| chr9:129141911-129142041 | Common:3; Rare:27 | ||||
| chr9:129803062-129803194 | Common:2; Rare:41 | ||||
| chr9:129824087-129824322 | Common:4; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835214-129835478 | Common:2; Rare:107 | ||||
| chr9:130053847-130053963 | Common:1; Rare:46 | ||||
| chr9:130476131-130476639 | Common:2; Rare:104 |