| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221940-99222355 | Common:2; Rare:154; Clinvar:2 | ||||
| chr9:99906591-99906684 | Rare:43 | ||||
| chr9:100098974-100099314 | Common:2; Rare:94; Clinvar:2 | ||||
| chr9:100352887-100353081 | Rare:65 | ||||
| chr9:101398570-101398895 | Common:1; Rare:113 | ||||
| chr9:101533690-101533894 | Rare:59 | ||||
| chr9:104093985-104094366 | Common:5; Rare:96 | ||||
| chr9:104094504-104094603 | Common:2; Rare:31 | ||||
| chr9:105558057-105558159 | Rare:33; Clinvar (benign):1 | ||||
| chr9:107282984-107283286 | Common:1; Rare:101 | ||||
| chr9:108933945-108934426 | Common:8; Rare:177; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:109498227-109498464 | Rare:74 | ||||
| chr9:111599623-111599898 | Common:2; Rare:78 | ||||
| chr9:111661481-111661673 | Common:3; Rare:56 | ||||
| chr9:111896640-111896777 | Common:3; Rare:52 |