| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086982-70087134 | Rare:67 | ||||
| chr2:70087437-70087750 | Rare:122 | ||||
| chr2:70293661-70293848 | Common:2; Rare:62 | ||||
| chr2:71068539-71068699 | Rare:68 | ||||
| chr2:71130225-71130662 | Common:6; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276462-71276599 | Rare:41 | ||||
| chr2:73071707-73071863 | Common:2; Rare:56 | ||||
| chr2:73214172-73214260 | Common:1; Rare:27 | ||||
| chr2:73234240-73234356 | Common:1; Rare:35 | ||||
| chr2:73737300-73737620 | Common:3; Rare:104 | ||||
| chr2:73828804-73829005 | Common:1; Rare:45 | ||||
| chr2:74147862-74148140 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74421579-74421759 | Rare:62 | ||||
| chr2:74440557-74440649 | Rare:21 | ||||
| chr2:74482928-74483095 | Common:1; Rare:56 |