| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152834927-152835146 | Common:2; Rare:65 | ||||
| chr3:154324444-154324595 | Rare:50 | ||||
| chr3:155870367-155870741 | Common:1; Rare:106 | ||||
| chr3:156674438-156674618 | Common:1; Rare:45 | ||||
| chr3:157160098-157160334 | Rare:99 | ||||
| chr3:158802011-158802146 | Common:2; Rare:64 | ||||
| chr3:160399196-160399309 | Rare:30; Clinvar:1 | ||||
| chr3:160399516-160399660 | Rare:29 | ||||
| chr3:160449752-160450027 | Common:2; Rare:86 | ||||
| chr3:167734837-167735181 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169663608-169663687 | Common:1; Rare:16 | ||||
| chr3:169773331-169773417 | Rare:25 | ||||
| chr3:169966632-169966851 | Common:2; Rare:85 | ||||
| chr3:170870175-170870304 | Rare:63 | ||||
| chr3:172039485-172039662 | Common:1; Rare:57 |