| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4320943-4321253 | Common:5; Rare:118 | ||||
| chr12:4538436-4538786 | Rare:74 | ||||
| chr12:4649019-4649154 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr12:6124569-6124890 | Rare:34 | ||||
| chr12:6200005-6200520 | Common:4; Rare:152 | ||||
| chr12:6375334-6375547 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6383995-6384250 | Common:1; Rare:56 | ||||
| chr12:6451785-6452120 | Common:4; Rare:62 | ||||
| chr12:6493175-6493386 | Common:7; Rare:62 | ||||
| chr12:6493763-6493902 | Common:2; Rare:43 | ||||
| chr12:6534252-6534582 | Common:6; Rare:132 | ||||
| chr12:6568253-6568382 | Rare:48 | ||||
| chr12:6688901-6689212 | Rare:100 | ||||
| chr12:6689471-6689748 | Common:1; Rare:67 |