| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158571052-158571229 | Rare:57 | ||||
| chr3:158801950-158802161 | Common:3; Rare:95 | ||||
| chr3:160399153-160399307 | Rare:38; Clinvar:2 | ||||
| chr3:160399512-160399676 | Rare:36 | ||||
| chr3:160449506-160449857 | Rare:102 | ||||
| chr3:160565528-160565785 | Common:2; Rare:100 | ||||
| chr3:161221202-161221330 | Rare:37 | ||||
| chr3:161371455-161371774 | Common:3; Rare:57 | ||||
| chr3:167734805-167735227 | Common:3; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735586-167735752 | Rare:41 | ||||
| chr3:169773313-169773424 | Rare:37 | ||||
| chr3:170181717-170181826 | Rare:43 | ||||
| chr3:170222302-170222560 | Common:2; Rare:83 | ||||
| chr3:170870163-170870323 | Rare:77 | ||||
| chr3:172711063-172711350 | Common:1; Rare:72 |