| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48119181-48119398 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350787-48350963 | Rare:64 | ||||
| chr12:48682185-48682421 | Common:5; Rare:77 | ||||
| chr12:48716666-48716928 | Common:4; Rare:85 | ||||
| chr12:48818583-48818818 | Common:1; Rare:84 | ||||
| chr12:48852093-48852378 | Common:2; Rare:83 | ||||
| chr12:48957367-48957669 | Common:4; Rare:83 | ||||
| chr12:49018741-49018933 | Common:1; Rare:79 | ||||
| chr12:49110840-49111041 | Rare:49 | ||||
| chr12:49131296-49131621 | Common:2; Rare:126 | ||||
| chr12:49188482-49188612 | Common:2; Rare:18 | ||||
| chr12:49188977-49189274 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322934-49323309 | Common:3; Rare:100 | ||||
| chr12:49366796-49367021 | Common:1; Rare:56 | ||||
| chr12:49367214-49367581 | Common:1; Rare:99 |