| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55927809-55928097 | Rare:79 | ||||
| chr12:55930884-55931209 | Common:1; Rare:53 | ||||
| chr12:55931915-55932101 | Rare:48 | ||||
| chr12:55958462-55958767 | Rare:94 | ||||
| chr12:55965987-55966178 | Common:1; Rare:42 | ||||
| chr12:55966653-55966904 | Rare:66 | ||||
| chr12:55973696-55973949 | Common:2; Rare:72 | ||||
| chr12:56007608-56007908 | Common:2; Rare:80 | ||||
| chr12:56020830-56021055 | Rare:42 | ||||
| chr12:56021194-56021361 | Common:9; Rare:23 | ||||
| chr12:56041613-56041972 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr12:56079622-56079923 | Rare:63 | ||||
| chr12:56104200-56104824 | Common:5; Rare:204 | ||||
| chr12:56116523-56116948 | Common:3; Rare:142 | ||||
| chr12:56117985-56118293 | Rare:99 |