| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55966700-55966885 | Rare:47 | ||||
| chr12:55997081-55997344 | Common:1; Rare:77; Clinvar:2 | ||||
| chr12:56041613-56042009 | Common:4; Rare:89; Clinvar (benign):1 | ||||
| chr12:56079973-56080220 | Common:4; Rare:62 | ||||
| chr12:56104365-56104779 | Common:5; Rare:145 | ||||
| chr12:56116525-56116704 | Common:2; Rare:78 | ||||
| chr12:56152460-56152620 | Rare:48 | ||||
| chr12:56158219-56158403 | Rare:61 | ||||
| chr12:56221856-56222026 | Common:1; Rare:43 | ||||
| chr12:56267064-56267319 | Common:2; Rare:64 | ||||
| chr12:56300013-56300163 | Common:2; Rare:57 | ||||
| chr12:56300287-56300624 | Common:3; Rare:92 | ||||
| chr12:56315821-56316111 | Common:1; Rare:72 | ||||
| chr12:56316147-56316249 | Rare:22 | ||||
| chr12:56333894-56334179 | Common:1; Rare:83 |