| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249524-129249704 | Common:2; Rare:55 | ||||
| chr3:129439852-129440300 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:132659796-132659981 | Common:3; Rare:44 | ||||
| chr3:133661896-133661998 | Rare:26 | ||||
| chr3:134485690-134485785 | Rare:39 | ||||
| chr3:134485971-134486140 | Common:2; Rare:52 | ||||
| chr3:136861990-136862298 | Common:1; Rare:100 | ||||
| chr3:139389567-139389828 | Common:1; Rare:83 | ||||
| chr3:141876319-141876660 | Common:1; Rare:107 | ||||
| chr3:143971694-143971837 | Common:1; Rare:68 | ||||
| chr3:146160896-146161075 | Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:150603149-150603305 | Common:1; Rare:49 | ||||
| chr3:156674337-156674627 | Common:4; Rare:86 | ||||
| chr3:158672424-158672744 | Common:3; Rare:95 | ||||
| chr3:160399207-160399516 | Rare:95; Clinvar:6 |