| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:67654562-67654754 | Common:2; Rare:77 | ||||
| chr3:69013200-69013389 | Rare:54 | ||||
| chr3:69013590-69013822 | Common:1; Rare:71 | ||||
| chr3:69080342-69080451 | Rare:48 | ||||
| chr3:69084755-69085072 | Common:3; Rare:80 | ||||
| chr3:69200386-69200633 | Common:2; Rare:40 | ||||
| chr3:69200695-69200955 | Common:1; Rare:65 | ||||
| chr3:69541264-69541390 | Common:1; Rare:21 | ||||
| chr3:79018819-79019012 | Rare:48 | ||||
| chr3:87227032-87227504 | Common:3; Rare:142; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058888-88059308 | Common:3; Rare:161 | ||||
| chr3:88149663-88149758 | Rare:20 | ||||
| chr3:88149816-88150042 | Common:4; Rare:80 | ||||
| chr3:93979922-93980195 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94028530-94028733 | Rare:34 |