| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170870175-170870304 | Rare:63 | ||||
| chr3:170908590-170908837 | Common:1; Rare:68 | ||||
| chr3:171101617-171101726 | Rare:26 | ||||
| chr3:171460320-171460571 | Rare:57 | ||||
| chr3:179147913-179148196 | Common:4; Rare:84 | ||||
| chr3:179347636-179347799 | Common:1; Rare:42 | ||||
| chr3:179562671-179563009 | Rare:109 | ||||
| chr3:179604630-179604848 | Common:2; Rare:76 | ||||
| chr3:179974054-179974336 | Common:2; Rare:41 | ||||
| chr3:180602106-180602384 | Common:1; Rare:98 | ||||
| chr3:180679467-180679552 | Rare:15; Clinvar:2 | ||||
| chr3:180951083-180951397 | Common:1; Rare:64 | ||||
| chr3:180989665-180989804 | Rare:55; Clinvar:1 | ||||
| chr3:181711736-181711986 | Rare:77 | ||||
| chr3:183099416-183099742 | Common:2; Rare:108; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 |