| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2798543-2798822 | Common:2; Rare:69 | ||||
| chr12:2876980-2877268 | Rare:89 | ||||
| chr12:2959164-2959480 | Common:1; Rare:82 | ||||
| chr12:2959843-2959958 | Common:1; Rare:29 | ||||
| chr12:3873355-3873512 | Common:1; Rare:35 | ||||
| chr12:4273460-4273773 | Rare:80 | ||||
| chr12:4274170-4274229 | Rare:7 | ||||
| chr12:4275749-4276056 | Rare:65 | ||||
| chr12:4320949-4321273 | Common:5; Rare:125 | ||||
| chr12:4538431-4538930 | Common:3; Rare:114 | ||||
| chr12:4648974-4649154 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr12:6375346-6375667 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376172-6376387 | Common:2; Rare:47 | ||||
| chr12:6493230-6493502 | Common:7; Rare:81 | ||||
| chr12:6493763-6494148 | Common:2; Rare:112 |