| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828387-49828575 | Common:1; Rare:69 | ||||
| chr12:50085157-50085364 | Common:1; Rare:57 | ||||
| chr12:50283473-50283629 | Rare:49 | ||||
| chr12:50763927-50764120 | Common:1; Rare:55 | ||||
| chr12:51173126-51173243 | Rare:22 | ||||
| chr12:51238658-51238893 | Common:8; Rare:105 | ||||
| chr12:52051153-52051457 | Common:1; Rare:99 | ||||
| chr12:52492649-52492681 | Rare:10; Clinvar (pathogenic):2 | ||||
| chr12:53079365-53079568 | Common:2; Rare:66 | ||||
| chr12:53625962-53626166 | Common:1; Rare:51 | ||||
| chr12:53986235-53986299 | Rare:21 | ||||
| chr12:54009552-54009663 | Common:1; Rare:39 | ||||
| chr12:54259535-54259727 | Rare:35 | ||||
| chr12:54385723-54386041 | Rare:57 | ||||
| chr12:55728954-55729164 | Rare:43 |