| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97983028-97983603 | Common:2; Rare:215 | ||||
| chr9:98119145-98119256 | Common:1; Rare:36 | ||||
| chr9:98119260-98119466 | Common:1; Rare:41 | ||||
| chr9:98255598-98255852 | Common:3; Rare:78 | ||||
| chr9:99221878-99222364 | Common:2; Rare:200; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:99906574-99906717 | Rare:67 | ||||
| chr9:100098946-100099342 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352818-100353089 | Rare:96 | ||||
| chr9:101028623-101028827 | Common:2; Rare:66 | ||||
| chr9:101398511-101398929 | Common:1; Rare:147 | ||||
| chr9:101435721-101435976 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:101533737-101533907 | Rare:57 | ||||
| chr9:104093752-104093783 | Common:1; Rare:10 | ||||
| chr9:104093985-104094317 | Common:3; Rare:78 | ||||
| chr9:104747559-104747802 | Common:1; Rare:73 |