| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63668616-63668741 | Common:4; Rare:38 | ||||
| chr12:63779723-63779915 | Common:3; Rare:68 | ||||
| chr12:63780077-63780175 | Rare:44; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:64222248-64222384 | Rare:44 | ||||
| chr12:64404178-64404669 | Common:6; Rare:174 | ||||
| chr12:64452032-64452174 | Common:1; Rare:51 | ||||
| chr12:64759373-64759501 | Common:1; Rare:42; Clinvar:3 | ||||
| chr12:65169456-65169611 | Common:1; Rare:54; Clinvar:2 | ||||
| chr12:65278478-65278833 | Common:3; Rare:123; Clinvar (benign):3 | ||||
| chr12:65823718-65823974 | Common:2; Rare:52 | ||||
| chr12:65824212-65824448 | Common:1; Rare:60 | ||||
| chr12:65824795-65824871 | Rare:19 | ||||
| chr12:65824932-65825273 | Rare:85 | ||||
| chr12:66130703-66130879 | Rare:58 | ||||
| chr12:66169952-66170096 | Common:1; Rare:39 |