| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64473833-64474088 | Rare:31 | ||||
| chr12:64497750-64498040 | Rare:60; Clinvar (pathogenic):1 | ||||
| chr12:64625771-64626007 | Common:1; Rare:53 | ||||
| chr12:65170247-65170360 | Rare:43; Clinvar:2 | ||||
| chr12:65283965-65284003 | Rare:5 | ||||
| chr12:65396835-65396956 | Rare:14 | ||||
| chr12:65455236-65455463 | Common:1; Rare:30 | ||||
| chr12:65466895-65467077 | Rare:25 | ||||
| chr12:65603753-65603817 | Rare:10 | ||||
| chr12:65826911-65827173 | Rare:51 | ||||
| chr12:65831315-65831356 | Rare:9 | ||||
| chr12:65832720-65832924 | Rare:29 | ||||
| chr12:65833341-65833387 | Rare:8 | ||||
| chr12:65834507-65834688 | Common:1; Rare:37 | ||||
| chr12:65837667-65837889 | Common:1; Rare:35 |