| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633282-97633423 | Rare:36 | ||||
| chr9:97697298-97697468 | Common:1; Rare:90; Clinvar:5 | ||||
| chr9:97922059-97922387 | Common:5; Rare:113 | ||||
| chr9:97922429-97922630 | Common:5; Rare:100 | ||||
| chr9:98119194-98119305 | Common:1; Rare:27 | ||||
| chr9:99221898-99222354 | Common:2; Rare:180; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99906518-99906721 | Common:1; Rare:86 | ||||
| chr9:100098960-100099305 | Common:3; Rare:95; Clinvar:1 | ||||
| chr9:100352873-100353083 | Rare:74 | ||||
| chr9:101398592-101398907 | Common:1; Rare:98 | ||||
| chr9:104094013-104094322 | Common:2; Rare:65 | ||||
| chr9:104747541-104747763 | Rare:59 | ||||
| chr9:104764057-104764179 | Common:2; Rare:28 | ||||
| chr9:105694377-105694553 | Common:3; Rare:67 | ||||
| chr9:108934055-108934468 | Common:7; Rare:161; Clinvar:2; Clinvar (benign):2 |