| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792376-9792499 | Rare:36 | ||||
| chr3:9792685-9793123 | Common:3; Rare:155 | ||||
| chr3:9843968-9844128 | Common:2; Rare:62 | ||||
| chr3:9933523-9933904 | Common:3; Rare:151; Clinvar:3 | ||||
| chr3:10011087-10011268 | Common:1; Rare:56 | ||||
| chr3:10026304-10026480 | Rare:57 | ||||
| chr3:10115520-10115737 | Common:3; Rare:80 | ||||
| chr3:10141647-10141887 | Common:3; Rare:109; Clinvar:21; Clinvar (benign):20 | ||||
| chr3:10142141-10142187 | Rare:17; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:10321043-10321279 | Common:2; Rare:94 | ||||
| chr3:10505483-10505836 | Common:2; Rare:67 | ||||
| chr3:11272247-11272413 | Common:1; Rare:32 | ||||
| chr3:11719432-11719581 | Rare:46 | ||||
| chr3:11846843-11846996 | Common:1; Rare:42 | ||||
| chr3:12004240-12004391 | Common:2; Rare:45 |