| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158801976-158802206 | Common:2; Rare:102 | ||||
| chr3:159763928-159764201 | Common:2; Rare:80 | ||||
| chr3:159764345-159764522 | Rare:49 | ||||
| chr3:159988421-159988870 | Common:1; Rare:83 | ||||
| chr3:160399168-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399512-160399712 | Rare:51 | ||||
| chr3:160449710-160449946 | Common:1; Rare:80 | ||||
| chr3:160565260-160565831 | Common:3; Rare:191 | ||||
| chr3:161105032-161105366 | Common:3; Rare:98 | ||||
| chr3:161221429-161221582 | Common:2; Rare:39 | ||||
| chr3:161371467-161371774 | Common:3; Rare:54 | ||||
| chr3:167734799-167735254 | Common:5; Rare:148; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735609-167735754 | Rare:37 | ||||
| chr3:169773362-169773440 | Rare:25 | ||||
| chr3:169966720-169966855 | Rare:60 |