| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98255593-98255899 | Common:3; Rare:92 | ||||
| chr9:99221890-99222349 | Common:2; Rare:181; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99906570-99906717 | Rare:68 | ||||
| chr9:100098966-100099332 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352860-100353078 | Rare:76 | ||||
| chr9:101398563-101398902 | Common:1; Rare:118 | ||||
| chr9:104093985-104094339 | Common:3; Rare:86 | ||||
| chr9:104094431-104094593 | Common:2; Rare:42 | ||||
| chr9:104747617-104747795 | Common:1; Rare:56 | ||||
| chr9:104747871-104747961 | Common:2; Rare:28 | ||||
| chr9:104928181-104928476 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105558060-105558163 | Rare:32; Clinvar (benign):1 | ||||
| chr9:106862965-106863180 | Rare:74 | ||||
| chr9:106863527-106863637 | Rare:22 | ||||
| chr9:107282948-107283292 | Common:3; Rare:121 |