| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55927798-55928114 | Rare:85 | ||||
| chr12:55931820-55932234 | Rare:84 | ||||
| chr12:55936345-55936455 | Rare:21 | ||||
| chr12:55952920-55953161 | Common:1; Rare:62 | ||||
| chr12:55966698-55966904 | Rare:54 | ||||
| chr12:55974438-55974514 | Rare:10 | ||||
| chr12:56041563-56041989 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr12:56104303-56104412 | Rare:30 | ||||
| chr12:56104434-56104828 | Common:5; Rare:138 | ||||
| chr12:56110390-56110397 | Rare:1 | ||||
| chr12:56110684-56110985 | Rare:78 | ||||
| chr12:56116474-56117045 | Common:4; Rare:184 | ||||
| chr12:56117081-56117221 | Common:4; Rare:38 | ||||
| chr12:56118000-56118290 | Rare:95 | ||||
| chr12:56130461-56130622 | Rare:44 |