| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96778040-96778156 | Rare:37 | ||||
| chr9:97633271-97633887 | Common:6; Rare:190 | ||||
| chr9:97697275-97697468 | Common:2; Rare:110; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922471-97922613 | Common:4; Rare:66 | ||||
| chr9:98056494-98056777 | Common:1; Rare:90 | ||||
| chr9:98192627-98192853 | Common:5; Rare:63 | ||||
| chr9:99221916-99222355 | Common:2; Rare:171; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99821664-99822065 | Rare:114 | ||||
| chr9:99906574-99906694 | Rare:62 | ||||
| chr9:100098951-100099314 | Common:3; Rare:103; Clinvar:2 | ||||
| chr9:100352831-100353089 | Rare:93 | ||||
| chr9:100427034-100427384 | Common:7; Rare:127 | ||||
| chr9:101028628-101029009 | Common:4; Rare:115 | ||||
| chr9:101398523-101398910 | Common:1; Rare:139 | ||||
| chr9:101487050-101487088 | Rare:16 |