| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63779749-63780133 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:64222233-64222346 | Rare:41 | ||||
| chr12:64452014-64452174 | Common:1; Rare:59 | ||||
| chr12:64759336-64759479 | Rare:47; Clinvar:3 | ||||
| chr12:66130703-66130861 | Rare:57 | ||||
| chr12:66169934-66170217 | Common:2; Rare:72 | ||||
| chr12:67649028-67649046 | Rare:5 | ||||
| chr12:68332265-68332644 | Common:1; Rare:127 | ||||
| chr12:68610704-68611041 | Common:1; Rare:144 | ||||
| chr12:68686813-68687023 | Common:4; Rare:60 | ||||
| chr12:68807968-68808249 | Common:3; Rare:91 | ||||
| chr12:68808472-68808476 | |||||
| chr12:68933158-68933339 | Rare:57 | ||||
| chr12:69470286-69470436 | Common:3; Rare:58 | ||||
| chr12:70243569-70243770 | Common:1; Rare:58 |