| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55728940-55729214 | Rare:59 | ||||
| chr12:55729657-55729801 | Rare:32 | ||||
| chr12:55829523-55829793 | Rare:88 | ||||
| chr12:55830744-55830925 | Rare:61 | ||||
| chr12:55931944-55932101 | Rare:41 | ||||
| chr12:55966679-55966843 | Rare:43 | ||||
| chr12:55997049-55997344 | Common:1; Rare:83; Clinvar:2 | ||||
| chr12:56041562-56041968 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr12:56079922-56080209 | Common:4; Rare:67 | ||||
| chr12:56083027-56083364 | Rare:46 | ||||
| chr12:56104206-56104674 | Common:4; Rare:155 | ||||
| chr12:56116560-56116813 | Common:1; Rare:91 | ||||
| chr12:56127925-56128295 | Rare:71 | ||||
| chr12:56152481-56152618 | Rare:39 | ||||
| chr12:56158216-56158403 | Rare:61 |