| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100098966-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352860-100353114 | Rare:93 | ||||
| chr9:101398563-101398910 | Common:1; Rare:119 | ||||
| chr9:101487050-101487166 | Rare:35 | ||||
| chr9:101533700-101533937 | Rare:71 | ||||
| chr9:104093977-104094369 | Common:5; Rare:100 | ||||
| chr9:104094509-104094623 | Common:2; Rare:38 | ||||
| chr9:104747649-104747763 | Rare:31 | ||||
| chr9:105558040-105558184 | Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862980-106863190 | Rare:73 | ||||
| chr9:108933950-108933989 | Common:1; Rare:17; Clinvar:4 | ||||
| chr9:108934074-108934478 | Common:7; Rare:162; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109013445-109013734 | Common:2; Rare:104 | ||||
| chr9:110256410-110256720 | Common:4; Rare:108 | ||||
| chr9:110668717-110668870 | Common:1; Rare:27; Clinvar:2 |