| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4648998-4649171 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:6124509-6124762 | Rare:36; Clinvar:2 | ||||
| chr12:6200042-6200559 | Common:4; Rare:152 | ||||
| chr12:6200638-6200735 | Common:1; Rare:24 | ||||
| chr12:6375364-6375567 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6383988-6384250 | Common:1; Rare:57 | ||||
| chr12:6451780-6452149 | Common:4; Rare:69 | ||||
| chr12:6493088-6493386 | Common:7; Rare:88 | ||||
| chr12:6493763-6494113 | Common:2; Rare:104 | ||||
| chr12:6568234-6568388 | Rare:59 | ||||
| chr12:6647396-6647539 | Rare:45 | ||||
| chr12:6688893-6688990 | Rare:24 | ||||
| chr12:6689409-6689748 | Common:2; Rare:91 | ||||
| chr12:6724011-6724172 | Rare:46 | ||||
| chr12:6724196-6724296 | Rare:21 |