| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906586-99906712 | Rare:57 | ||||
| chr9:100098970-100099322 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352851-100353089 | Rare:86 | ||||
| chr9:100429408-100429629 | Rare:36 | ||||
| chr9:101398588-101398907 | Common:1; Rare:101 | ||||
| chr9:101487034-101487225 | Common:2; Rare:51 | ||||
| chr9:105244365-105244647 | Common:1; Rare:97 | ||||
| chr9:105558041-105558179 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862958-106863180 | Rare:74 | ||||
| chr9:106863495-106863645 | Common:1; Rare:29 | ||||
| chr9:108933921-108934493 | Common:9; Rare:224; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:109013446-109013669 | Common:2; Rare:83 | ||||
| chr9:110256414-110256729 | Common:5; Rare:110 | ||||
| chr9:111036137-111036240 | Rare:21 | ||||
| chr9:111036247-111036555 | Common:5; Rare:48 |