| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12725600-12725965 | Common:4; Rare:84 | ||||
| chr12:12891314-12891575 | Common:1; Rare:50 | ||||
| chr12:14365495-14365763 | Common:1; Rare:85 | ||||
| chr12:14771124-14771244 | Rare:38 | ||||
| chr12:14774184-14774698 | Common:3; Rare:162 | ||||
| chr12:14803414-14803715 | Common:2; Rare:82 | ||||
| chr12:14885717-14885968 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:15221253-15221539 | Common:1; Rare:78 | ||||
| chr12:15882319-15882620 | Common:1; Rare:82 | ||||
| chr12:20369558-20369921 | Common:3; Rare:165 | ||||
| chr12:21501565-21501880 | Common:1; Rare:79 | ||||
| chr12:21940949-21941389 | Rare:85 | ||||
| chr12:21941394-21941491 | Rare:21 | ||||
| chr12:22334687-22334740 | Common:1; Rare:10 | ||||
| chr12:22544164-22544292 | Common:1; Rare:62 |