| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96655295-96655408 | Rare:30 | ||||
| chr9:97039069-97039282 | Rare:81 | ||||
| chr9:97633312-97633458 | Common:1; Rare:40 | ||||
| chr9:97633467-97633848 | Common:5; Rare:123 | ||||
| chr9:97697304-97697489 | Common:1; Rare:94; Clinvar:5 | ||||
| chr9:97922463-97922642 | Common:4; Rare:86 | ||||
| chr9:98056567-98056789 | Common:2; Rare:78 | ||||
| chr9:98192623-98192824 | Common:5; Rare:57 | ||||
| chr9:98255306-98255395 | Rare:19 | ||||
| chr9:99221906-99222357 | Common:2; Rare:176; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906583-99906711 | Rare:61 | ||||
| chr9:100098972-100099327 | Common:3; Rare:98; Clinvar:2 | ||||
| chr9:100352854-100353081 | Rare:82 | ||||
| chr9:100429408-100429619 | Rare:35 | ||||
| chr9:101398580-101398905 | Common:1; Rare:107 |