| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37422564-37422781 | Common:4; Rare:198; Clinvar:1 | ||||
| chr9:37464920-37465150 | Common:3; Rare:95 | ||||
| chr9:37465170-37465660 | Common:6; Rare:244 | ||||
| chr9:37465694-37465975 | Common:1; Rare:111 | ||||
| chr9:37485730-37486055 | Common:5; Rare:211 | ||||
| chr9:37592478-37592698 | Common:4; Rare:118 | ||||
| chr9:37784932-37785166 | Common:2; Rare:167; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:37800583-37800953 | Common:5; Rare:235 | ||||
| chr9:37904020-37904252 | Common:4; Rare:125 | ||||
| chr9:38069189-38069449 | Common:9; Rare:179 | ||||
| chr9:38392579-38392871 | Common:2; Rare:128 | ||||
| chr9:38620460-38620910 | Common:5; Rare:183 | ||||
| chr9:68779946-68780112 | Common:4; Rare:101 | ||||
| chr9:69121199-69121608 | Common:2; Rare:166 | ||||
| chr9:69173890-69174300 | Common:11; Rare:198 |