| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55742900-55743350 | Rare:84 | ||||
| chr12:55829460-55829804 | Rare:194 | ||||
| chr12:55830450-55830980 | Common:3; Rare:204 | ||||
| chr12:55926810-55927020 | Common:1; Rare:52 | ||||
| chr12:55927809-55928119 | Rare:154 | ||||
| chr12:55966682-55966880 | Rare:99 | ||||
| chr12:55974160-55974650 | Common:2; Rare:97 | ||||
| chr12:55997055-55997373 | Common:3; Rare:169; Clinvar:4 | ||||
| chr12:56007230-56007560 | Common:1; Rare:91 | ||||
| chr12:56020720-56021150 | Common:1; Rare:126 | ||||
| chr12:56021190-56021740 | Common:22; Rare:264 | ||||
| chr12:56041563-56042190 | Common:12; Rare:325; Clinvar:6; Clinvar (benign):12 | ||||
| chr12:56079300-56079560 | Rare:49 | ||||
| chr12:56079622-56079932 | Rare:101 | ||||
| chr12:56079970-56080308 | Common:6; Rare:150 |