| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35731943-35732724 | Common:10; Rare:364 | ||||
| chr9:35748958-35749392 | Common:3; Rare:262 | ||||
| chr9:35813753-35814473 | Rare:180 | ||||
| chr9:35814961-35815302 | Rare:168 | ||||
| chr9:35815340-35815710 | Common:6; Rare:154 | ||||
| chr9:35829124-35829283 | Common:1; Rare:43 | ||||
| chr9:36036800-36036967 | Common:1; Rare:59 | ||||
| chr9:36190694-36191047 | Common:4; Rare:214 | ||||
| chr9:36257780-36258110 | Common:6; Rare:60 | ||||
| chr9:36258340-36258646 | Common:5; Rare:137; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:36400200-36400530 | Common:6; Rare:168 | ||||
| chr9:36400820-36401012 | Common:6; Rare:156 | ||||
| chr9:36487560-36488000 | Common:3; Rare:275 | ||||
| chr9:36572731-36573053 | Common:3; Rare:157 | ||||
| chr9:37120126-37120630 | Common:4; Rare:306 |