| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56079769-56079880 | Rare:28 | ||||
| chr12:56079973-56080378 | Common:4; Rare:104 | ||||
| chr12:56087792-56088169 | Common:2; Rare:100; Clinvar (pathogenic):1 | ||||
| chr12:56097626-56097934 | Rare:78 | ||||
| chr12:56098384-56098575 | Common:1; Rare:39 | ||||
| chr12:56104364-56104825 | Common:5; Rare:157 | ||||
| chr12:56116377-56116825 | Common:3; Rare:164 | ||||
| chr12:56118094-56118290 | Rare:61 | ||||
| chr12:56128177-56128366 | Rare:57 | ||||
| chr12:56152481-56152630 | Rare:45 | ||||
| chr12:56157624-56157734 | Common:1; Rare:33 | ||||
| chr12:56158237-56158415 | Rare:63 | ||||
| chr12:56161869-56162257 | Common:2; Rare:80 | ||||
| chr12:56178693-56179031 | Rare:106 | ||||
| chr12:56221846-56222026 | Common:1; Rare:47 |