| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:171460771-171460959 | Rare:45 | ||||
| chr3:172039551-172039683 | Common:1; Rare:51 | ||||
| chr3:172040396-172040608 | Common:1; Rare:50 | ||||
| chr3:172523352-172523595 | Common:1; Rare:64 | ||||
| chr3:172750893-172751026 | Rare:42 | ||||
| chr3:173396368-173396633 | Common:2; Rare:48 | ||||
| chr3:173397620-173397857 | Rare:90 | ||||
| chr3:174440819-174441018 | Common:2; Rare:54 | ||||
| chr3:177196398-177196666 | Rare:84 | ||||
| chr3:179347545-179347795 | Common:2; Rare:60 | ||||
| chr3:179562632-179563003 | Rare:126 | ||||
| chr3:179604614-179604949 | Common:3; Rare:129 | ||||
| chr3:179652908-179653341 | Common:3; Rare:126 | ||||
| chr3:180602117-180602258 | Common:1; Rare:53 | ||||
| chr3:180989609-180989804 | Rare:85; Clinvar:1; Clinvar (benign):1 |