| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52032950-52033237 | Common:1; Rare:83 | ||||
| chr12:53465832-53465973 | Rare:28 | ||||
| chr12:55688023-55688148 | Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:55697215-55697477 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr12:55709758-55710083 | Common:4; Rare:48 | ||||
| chr12:56117289-56117578 | Common:2; Rare:70 | ||||
| chr12:57177235-57177557 | Common:1; Rare:82 | ||||
| chr12:57184185-57184366 | Rare:42 | ||||
| chr12:57204516-57204749 | Common:2; Rare:71 | ||||
| chr12:57211946-57212261 | Common:1; Rare:83 | ||||
| chr12:62603424-62603625 | Common:1; Rare:73 | ||||
| chr12:70550054-70550324 | Common:3; Rare:44 | ||||
| chr12:92466740-92466938 | Common:3; Rare:37 | ||||
| chr12:98503835-98503973 | Common:2; Rare:42 | ||||
| chr12:101761243-101761526 | Rare:59; Clinvar (pathogenic):2 |