| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32571190-32571480 | Common:2; Rare:44 | ||||
| chr3:32684779-32685714 | Rare:739 | ||||
| chr3:32685642-32686200 | Common:5; Rare:198 | ||||
| chr3:32951229-32951712 | Common:5; Rare:291 | ||||
| chr3:33096428-33096828 | Common:3; Rare:113 | ||||
| chr3:33096741-33096872 | Rare:39 | ||||
| chr3:33097010-33097573 | Common:15; Rare:566; Clinvar:19; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr3:33113518-33114200 | Common:9; Rare:465; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr3:33114350-33114840 | Common:11; Rare:728; Clinvar:28; Clinvar (benign):21; Clinvar (pathogenic):12 | ||||
| chr3:33115090-33115550 | Common:1; Rare:139 | ||||
| chr3:33277220-33277540 | Common:9; Rare:253 | ||||
| chr3:33439595-33440189 | Common:3; Rare:399 | ||||
| chr3:33440258-33441757 | Common:34; Rare:1408 | ||||
| chr3:33658962-33659995 | Common:9; Rare:461 | ||||
| chr3:33717490-33717930 | Common:2; Rare:143 |