| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68157515-68157949 | Common:2; Rare:223 | ||||
| chr2:68467274-68467616 | Common:1; Rare:89 | ||||
| chr2:69643622-69643855 | Rare:88 | ||||
| chr2:70293665-70293899 | Common:3; Rare:74 | ||||
| chr2:71068539-71068672 | Rare:59 | ||||
| chr2:71130220-71130662 | Common:6; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276457-71276618 | Rare:56 | ||||
| chr2:72144463-72144732 | Common:3; Rare:60 | ||||
| chr2:73071707-73071841 | Common:2; Rare:49 | ||||
| chr2:73233200-73233464 | Common:1; Rare:69 | ||||
| chr2:73234193-73234361 | Common:2; Rare:50 | ||||
| chr2:73828804-73829037 | Common:1; Rare:54 | ||||
| chr2:74147855-74148062 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178834-74179066 | Common:3; Rare:72 | ||||
| chr2:74421645-74421759 | Rare:35 |