| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152269543-152269696 | Rare:41 | ||||
| chr3:152298700-152298851 | Rare:22 | ||||
| chr3:154121264-154121451 | Common:2; Rare:80 | ||||
| chr3:155854350-155854614 | Rare:70 | ||||
| chr3:156674438-156674647 | Common:1; Rare:56 | ||||
| chr3:157160092-157160288 | Rare:85 | ||||
| chr3:158802016-158802155 | Common:2; Rare:64 | ||||
| chr3:160399164-160399307 | Rare:37; Clinvar:2 | ||||
| chr3:160399514-160399669 | Rare:34 | ||||
| chr3:160565548-160565842 | Common:2; Rare:100 | ||||
| chr3:161105289-161105360 | Common:1; Rare:29 | ||||
| chr3:161221217-161221330 | Rare:33 | ||||
| chr3:167734820-167735254 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735617-167735752 | Rare:34 | ||||
| chr3:169147108-169147518 | Common:2; Rare:96 |