| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633271-97633848 | Common:6; Rare:177 | ||||
| chr9:97922439-97922607 | Common:3; Rare:87 | ||||
| chr9:98056550-98056791 | Common:2; Rare:85 | ||||
| chr9:99221898-99222355 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99906600-99906694 | Rare:48 | ||||
| chr9:100098966-100099319 | Common:3; Rare:101; Clinvar:2 | ||||
| chr9:100352831-100353081 | Rare:90 | ||||
| chr9:101398575-101398912 | Common:1; Rare:112 | ||||
| chr9:101533755-101533899 | Rare:41 | ||||
| chr9:104094481-104094603 | Common:2; Rare:39 | ||||
| chr9:104747608-104747767 | Rare:44 | ||||
| chr9:105558003-105558170 | Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862980-106863180 | Rare:69 | ||||
| chr9:107488434-107488574 | Common:1; Rare:43 | ||||
| chr9:107489767-107490085 | Common:4; Rare:141 |