| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221890-99222358 | Common:2; Rare:187; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99821670-99822014 | Rare:98 | ||||
| chr9:99822016-99822070 | Rare:15 | ||||
| chr9:99906570-99906717 | Rare:68 | ||||
| chr9:100098958-100099359 | Common:4; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352823-100353114 | Rare:105 | ||||
| chr9:100426614-100426729 | Common:1; Rare:19 | ||||
| chr9:100427120-100427393 | Common:3; Rare:98 | ||||
| chr9:100429423-100429624 | Rare:33 | ||||
| chr9:101398505-101398905 | Common:1; Rare:143 | ||||
| chr9:101487043-101487236 | Common:3; Rare:53 | ||||
| chr9:101533737-101533914 | Rare:58 | ||||
| chr9:104093957-104094381 | Common:7; Rare:117 | ||||
| chr9:104094516-104094659 | Common:2; Rare:48 | ||||
| chr9:104747622-104747820 | Common:1; Rare:64 |