| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6200092-6200416 | Common:3; Rare:92 | ||||
| chr12:6383968-6384276 | Common:2; Rare:74 | ||||
| chr12:6470672-6470839 | Rare:40 | ||||
| chr12:6493175-6493381 | Common:7; Rare:61 | ||||
| chr12:6493742-6494119 | Common:2; Rare:111 | ||||
| chr12:6536463-6536788 | Rare:114 | ||||
| chr12:6549138-6549264 | Common:1; Rare:22 | ||||
| chr12:6568234-6568382 | Rare:55 | ||||
| chr12:6663100-6663413 | Common:2; Rare:88 | ||||
| chr12:6723920-6724172 | Common:1; Rare:62 | ||||
| chr12:6724230-6724296 | Rare:13 | ||||
| chr12:6752927-6753189 | Common:6; Rare:79 | ||||
| chr12:6851877-6852180 | Rare:81 | ||||
| chr12:6867365-6867615 | Common:2; Rare:122; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873330-6873541 | Common:1; Rare:58 |