| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906575-99906703 | Rare:64 | ||||
| chr9:100098972-100099314 | Common:3; Rare:94; Clinvar:2 | ||||
| chr9:100352858-100353089 | Rare:83 | ||||
| chr9:101398564-101398902 | Common:1; Rare:117 | ||||
| chr9:101487050-101487221 | Common:2; Rare:47 | ||||
| chr9:101533644-101533894 | Common:2; Rare:77 | ||||
| chr9:104094430-104094651 | Common:3; Rare:63 | ||||
| chr9:105558067-105558159 | Rare:28; Clinvar (benign):1 | ||||
| chr9:105694406-105694627 | Common:3; Rare:97 | ||||
| chr9:106862981-106863180 | Rare:68 | ||||
| chr9:108933989-108934025 | Rare:12 | ||||
| chr9:108934065-108934493 | Common:7; Rare:170; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110127324-110127467 | Rare:20 | ||||
| chr9:110256431-110256720 | Common:4; Rare:105 | ||||
| chr9:111038195-111038392 | Common:2; Rare:59 |