| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433799-58434029 | Common:1; Rare:82; Clinvar (benign):3 | ||||
| chr3:62318890-62319075 | Rare:76 | ||||
| chr3:63863777-63864126 | Common:7; Rare:116 | ||||
| chr3:63864418-63864540 | Common:2; Rare:42 | ||||
| chr3:67654582-67654727 | Common:1; Rare:51 | ||||
| chr3:69013590-69013812 | Common:1; Rare:67 | ||||
| chr3:88058935-88059294 | Common:2; Rare:133 | ||||
| chr3:88149605-88150036 | Common:5; Rare:121 | ||||
| chr3:94062897-94063027 | Rare:37 | ||||
| chr3:97764439-97764795 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr3:98901107-98901201 | Common:2; Rare:39 | ||||
| chr3:98901647-98901990 | Common:1; Rare:129 | ||||
| chr3:99638324-99638616 | Common:1; Rare:62 | ||||
| chr3:99817578-99817934 | Rare:109 | ||||
| chr3:100260905-100261021 | Rare:31 |