| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3873355-3873535 | Common:1; Rare:40 | ||||
| chr12:4276197-4276261 | Rare:18 | ||||
| chr12:4320943-4321258 | Common:5; Rare:120 | ||||
| chr12:4538440-4538927 | Common:3; Rare:109 | ||||
| chr12:4649010-4649178 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:4909725-4909918 | Common:2; Rare:40 | ||||
| chr12:5431948-5432118 | Common:4; Rare:67 | ||||
| chr12:6470894-6471051 | Common:2; Rare:33 | ||||
| chr12:6493234-6493398 | Common:6; Rare:45 | ||||
| chr12:6493770-6494138 | Common:2; Rare:110 | ||||
| chr12:6534172-6534594 | Common:6; Rare:158 | ||||
| chr12:6534640-6534860 | Common:3; Rare:88 | ||||
| chr12:6535132-6535309 | Common:2; Rare:65 | ||||
| chr12:6568260-6568388 | Rare:50 | ||||
| chr12:6603123-6603234 | Rare:25 |