| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:62318935-62319049 | Rare:43 | ||||
| chr3:63863774-63864161 | Common:8; Rare:129 | ||||
| chr3:63911991-63912094 | Rare:32 | ||||
| chr3:64687996-64688109 | Rare:31 | ||||
| chr3:67654576-67654778 | Common:2; Rare:77 | ||||
| chr3:69013579-69013824 | Common:1; Rare:74 | ||||
| chr3:69084773-69085072 | Common:3; Rare:78 | ||||
| chr3:71130558-71130661 | Rare:41; Clinvar:1 | ||||
| chr3:81761487-81761810 | Common:8; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:87227210-87227482 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058935-88059294 | Common:2; Rare:133 | ||||
| chr3:88149628-88150043 | Common:5; Rare:124 | ||||
| chr3:94062897-94063020 | Rare:37 | ||||
| chr3:97821908-97822074 | Rare:61 | ||||
| chr3:97972390-97972716 | Common:9; Rare:72 |