| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35079908-35080172 | Common:10; Rare:135; Clinvar:6; Clinvar (benign):8 | ||||
| chr9:35096532-35096748 | Common:2; Rare:86 | ||||
| chr9:35103054-35103288 | Common:2; Rare:144 | ||||
| chr9:35111325-35112044 | Common:2; Rare:253 | ||||
| chr9:35115844-35116138 | Common:1; Rare:54 | ||||
| chr9:35161786-35162178 | Common:8; Rare:182 | ||||
| chr9:35489606-35490164 | Common:6; Rare:247 | ||||
| chr9:35605122-35605303 | Common:2; Rare:109 | ||||
| chr9:35646750-35647200 | Common:5; Rare:150 | ||||
| chr9:35657877-35658356 | Common:14; Rare:793; Clinvar:72; Clinvar (benign):28; Clinvar (pathogenic):74 | ||||
| chr9:35665096-35665359 | Common:6; Rare:175 | ||||
| chr9:35673719-35673977 | Common:4; Rare:104 | ||||
| chr9:35685130-35685630 | Common:1; Rare:189; Clinvar:2; Clinvar (benign):7 | ||||
| chr9:35689753-35690120 | Common:7; Rare:192; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:35690604-35690725 | Rare:22 |