| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20622418-20622717 | Common:1; Rare:188 | ||||
| chr9:20684052-20684293 | Common:7; Rare:173 | ||||
| chr9:21335325-21335551 | Common:6; Rare:134 | ||||
| chr9:21802512-21802744 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:21974684-21975250 | Common:6; Rare:268; Clinvar:51; Clinvar (benign):29; Clinvar (pathogenic):5 | ||||
| chr9:21994069-21994912 | Common:4; Rare:468; Clinvar:42; Clinvar (benign):34; Clinvar (pathogenic):4 | ||||
| chr9:21994845-21995159 | Common:2; Rare:101 | ||||
| chr9:21995307-21995558 | Rare:136 | ||||
| chr9:22008689-22008831 | Rare:120 | ||||
| chr9:22009233-22009648 | Common:4; Rare:194 | ||||
| chr9:25678228-25678563 | Common:2; Rare:190 | ||||
| chr9:26892180-26892660 | Common:4; Rare:312 | ||||
| chr9:26892713-26892909 | Common:2; Rare:170 | ||||
| chr9:26946550-26947010 | Common:4; Rare:259; Clinvar (pathogenic):2 | ||||
| chr9:26947079-26947572 | Common:4; Rare:323 |