| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35691063-35691174 | Rare:23 | ||||
| chr9:35732089-35732683 | Common:8; Rare:315 | ||||
| chr9:35748882-35749402 | Common:5; Rare:323 | ||||
| chr9:35814215-35814466 | Rare:86 | ||||
| chr9:35814961-35815297 | Rare:149 | ||||
| chr9:35829030-35829293 | Common:4; Rare:107 | ||||
| chr9:36190676-36191064 | Common:3; Rare:222 | ||||
| chr9:36258359-36258630 | Common:4; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:36400700-36401150 | Common:6; Rare:226 | ||||
| chr9:36487588-36487849 | Common:1; Rare:181 | ||||
| chr9:36572731-36572948 | Common:1; Rare:117 | ||||
| chr9:37120126-37120638 | Common:4; Rare:295 | ||||
| chr9:37422532-37422777 | Common:4; Rare:203; Clinvar:1 | ||||
| chr9:37465120-37465960 | Common:7; Rare:415 | ||||
| chr9:37485684-37486045 | Common:7; Rare:235 |