| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2959784-2959985 | Common:2; Rare:51 | ||||
| chr12:4320949-4321298 | Common:5; Rare:136 | ||||
| chr12:4538430-4538947 | Common:3; Rare:121 | ||||
| chr12:4649013-4649159 | Common:2; Rare:52; Clinvar (benign):2 | ||||
| chr12:6200092-6200416 | Common:3; Rare:92 | ||||
| chr12:6451771-6452141 | Common:4; Rare:67 | ||||
| chr12:6470634-6470931 | Common:2; Rare:87 | ||||
| chr12:6493075-6493403 | Common:7; Rare:96 | ||||
| chr12:6493835-6494138 | Common:2; Rare:89 | ||||
| chr12:6533477-6533566 | Rare:18 | ||||
| chr12:6534317-6534861 | Common:8; Rare:225 | ||||
| chr12:6536450-6536745 | Rare:112 | ||||
| chr12:6549089-6549264 | Common:1; Rare:35 | ||||
| chr12:6568236-6568369 | Rare:50 | ||||
| chr12:6591474-6591696 | Rare:55 |