| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013570-69014330 | Common:10; Rare:786 | ||||
| chr3:69051425-69052045 | Common:4; Rare:171 | ||||
| chr3:69052068-69052637 | Common:41; Rare:866 | ||||
| chr3:69079481-69080634 | Common:12; Rare:752 | ||||
| chr3:69084443-69084603 | Rare:35 | ||||
| chr3:69084605-69085090 | Common:15; Rare:375 | ||||
| chr3:69085200-69085822 | Rare:200 | ||||
| chr3:69200740-69201140 | Common:2; Rare:183 | ||||
| chr3:69738934-69739049 | Rare:22 | ||||
| chr3:69739164-69739580 | Common:1; Rare:568 | ||||
| chr3:69866012-69866412 | Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:71063954-71065192 | Common:17; Rare:1128 | ||||
| chr3:71065414-71065814 | Common:1; Rare:84 | ||||
| chr3:71066243-71066643 | Common:3; Rare:96 | ||||
| chr3:71129790-71130951 | Common:7; Rare:832; Clinvar:14 |