| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25428106-25428419 | Rare:70 | ||||
| chr3:25783377-25783627 | Common:2; Rare:84; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:28241428-28241791 | Common:2; Rare:127 | ||||
| chr3:28348779-28349202 | Common:4; Rare:134 | ||||
| chr3:29280831-29281367 | Common:15; Rare:104 | ||||
| chr3:30894598-30894779 | Common:2; Rare:66 | ||||
| chr3:31532371-31532654 | Common:4; Rare:81 | ||||
| chr3:32106401-32106697 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502699-32502924 | Rare:69 | ||||
| chr3:32570651-32570962 | Common:1; Rare:138 | ||||
| chr3:32685079-32685456 | Rare:105 | ||||
| chr3:33097097-33097265 | Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33218795-33219012 | Common:3; Rare:64 | ||||
| chr3:33277289-33277513 | Common:3; Rare:68 |