| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101487020-101487185 | Common:1; Rare:48 | ||||
| chr9:101487193-101487229 | Common:1; Rare:7 | ||||
| chr9:101533748-101533914 | Rare:53 | ||||
| chr9:104093985-104094603 | Common:10; Rare:156 | ||||
| chr9:104747604-104747788 | Common:1; Rare:56 | ||||
| chr9:105447966-105448153 | Common:2; Rare:70 | ||||
| chr9:105558044-105558163 | Rare:40; Clinvar (benign):1 | ||||
| chr9:106862983-106863186 | Rare:67 | ||||
| chr9:106863501-106863660 | Common:1; Rare:30 | ||||
| chr9:107283971-107284125 | Common:1; Rare:49 | ||||
| chr9:107488357-107488617 | Common:1; Rare:65 | ||||
| chr9:108933911-108933985 | Common:2; Rare:24; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:108933988-108934493 | Common:7; Rare:199; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013459-109013768 | Common:2; Rare:111 | ||||
| chr9:109498227-109498517 | Common:1; Rare:84 |