| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633511-97633848 | Common:4; Rare:107 | ||||
| chr9:97922471-97922609 | Common:3; Rare:64 | ||||
| chr9:97983153-97983423 | Common:1; Rare:106 | ||||
| chr9:98192630-98192896 | Common:6; Rare:71 | ||||
| chr9:98943481-98943585 | Rare:17 | ||||
| chr9:98943685-98944003 | Common:4; Rare:95 | ||||
| chr9:99221892-99222365 | Common:2; Rare:191; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:99821695-99822031 | Rare:93 | ||||
| chr9:99906563-99906717 | Rare:69 | ||||
| chr9:100098974-100099336 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352858-100353081 | Rare:80 | ||||
| chr9:101398526-101398910 | Common:1; Rare:139 | ||||
| chr9:104093985-104094312 | Common:3; Rare:77 | ||||
| chr9:104747522-104747782 | Common:1; Rare:73 | ||||
| chr9:105558079-105558153 | Rare:17 |