| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97697249-97697468 | Common:2; Rare:128; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922471-97922606 | Common:3; Rare:63 | ||||
| chr9:97983172-97983441 | Common:1; Rare:107 | ||||
| chr9:98192605-98192879 | Common:6; Rare:75 | ||||
| chr9:99221897-99222356 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99906570-99906717 | Rare:68 | ||||
| chr9:100098949-100099314 | Common:3; Rare:103; Clinvar:2 | ||||
| chr9:100352854-100353103 | Rare:92 | ||||
| chr9:101028628-101029035 | Common:4; Rare:123 | ||||
| chr9:101398502-101398800 | Rare:116 | ||||
| chr9:101487043-101487195 | Common:2; Rare:44 | ||||
| chr9:101487197-101487248 | Common:1; Rare:11 | ||||
| chr9:101533720-101533907 | Rare:59 | ||||
| chr9:101738580-101738976 | Rare:83 | ||||
| chr9:104093985-104094381 | Common:5; Rare:101 |