| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128680633-128680916 | Common:3; Rare:94 | ||||
| chr3:128726032-128726242 | Common:1; Rare:63; Clinvar:3 | ||||
| chr3:128726825-128727005 | Rare:45 | ||||
| chr3:128879408-128879704 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160995-129161122 | Rare:50 | ||||
| chr3:129161217-129161477 | Common:1; Rare:72 | ||||
| chr3:129183774-129184129 | Common:2; Rare:133 | ||||
| chr3:129249544-129249739 | Common:1; Rare:55 | ||||
| chr3:129278761-129278900 | Common:4; Rare:43 | ||||
| chr3:129316283-129316317 | Rare:17 | ||||
| chr3:129439829-129440392 | Common:1; Rare:172; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893379-129893447 | Rare:21 | ||||
| chr3:129893523-129893887 | Rare:138 | ||||
| chr3:130746792-130746913 | Common:3; Rare:38 | ||||
| chr3:130893938-130894231 | Common:3; Rare:90 |