| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35657841-35658403 | Common:11; Rare:459; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35665171-35665286 | Common:1; Rare:46 | ||||
| chr9:35685289-35685703 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:35689702-35690152 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35690196-35690273 | Rare:16 | ||||
| chr9:35732073-35732364 | Common:2; Rare:87 | ||||
| chr9:35732373-35732684 | Common:3; Rare:79 | ||||
| chr9:35748978-35749392 | Common:2; Rare:153 | ||||
| chr9:35812146-35812381 | Rare:79 | ||||
| chr9:35814983-35815301 | Rare:82 | ||||
| chr9:35815425-35815574 | Common:1; Rare:35 | ||||
| chr9:35829068-35829290 | Common:1; Rare:58 | ||||
| chr9:35829366-35829532 | Common:1; Rare:38 | ||||
| chr9:36036754-36036980 | Common:3; Rare:75 | ||||
| chr9:36190676-36191000 | Common:1; Rare:108 |