| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35489747-35490144 | Common:3; Rare:121 | ||||
| chr9:35563838-35564133 | Common:1; Rare:85 | ||||
| chr9:35618346-35618717 | Common:3; Rare:86 | ||||
| chr9:35646801-35646943 | Rare:32 | ||||
| chr9:35650900-35651031 | Rare:38 | ||||
| chr9:35657841-35658491 | Common:11; Rare:483; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35689834 | Rare:35; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35689836-35690099 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35690659-35690838 | Rare:41 | ||||
| chr9:35691064-35691258 | Common:1; Rare:41 | ||||
| chr9:35732073-35732285 | Common:1; Rare:56 | ||||
| chr9:35732290-35732743 | Common:4; Rare:125 | ||||
| chr9:35748955-35749408 | Common:3; Rare:162 | ||||
| chr9:35812146-35812286 | Rare:56 | ||||
| chr9:35814975-35815302 | Rare:83 |