| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:30606391-30606699 | Common:1; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:31531879-31532244 | Common:6; Rare:109 | ||||
| chr3:31532250-31533026 | Common:8; Rare:274 | ||||
| chr3:31533610-31533789 | Common:3; Rare:46 | ||||
| chr3:32106321-32106696 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32391436-32391671 | Rare:38 | ||||
| chr3:32391774-32391922 | Common:3; Rare:41 | ||||
| chr3:32502313-32502538 | Common:3; Rare:54 | ||||
| chr3:32502696-32502955 | Rare:75 | ||||
| chr3:32570075-32570422 | Common:3; Rare:139 | ||||
| chr3:32570663-32571185 | Common:3; Rare:189 | ||||
| chr3:32571204-32571260 | Rare:10 | ||||
| chr3:32684984-32685402 | Rare:118 | ||||
| chr3:32817900-32818122 | Common:1; Rare:76 | ||||
| chr3:33096539-33096660 | Common:2; Rare:23 |