| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100352823-100353089 | Rare:94 | ||||
| chr9:101398526-101398912 | Common:1; Rare:140 | ||||
| chr9:101487043-101487088 | Rare:18 | ||||
| chr9:101533664-101533914 | Common:2; Rare:79 | ||||
| chr9:104093976-104094350 | Common:3; Rare:95 | ||||
| chr9:104094504-104094603 | Common:2; Rare:31 | ||||
| chr9:104747535-104747811 | Common:1; Rare:83 | ||||
| chr9:105558044-105558163 | Rare:40; Clinvar (benign):1 | ||||
| chr9:108933931-108934003 | Common:2; Rare:29; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:108934042-108934493 | Common:7; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:110048509-110048792 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chr9:110256410-110256693 | Common:3; Rare:101 | ||||
| chr9:111631132-111631338 | Rare:45 | ||||
| chr9:111661481-111661673 | Common:3; Rare:56 | ||||
| chr9:112379798-112380179 | Common:3; Rare:146 |