| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501474-21501938 | Common:6; Rare:142 | ||||
| chr12:21657739-21657891 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22544142-22544263 | Rare:57 | ||||
| chr12:22544444-22544721 | Common:2; Rare:65 | ||||
| chr12:22625013-22625216 | Common:1; Rare:100 | ||||
| chr12:24948943-24949295 | Common:4; Rare:81 | ||||
| chr12:24949300-24949486 | Rare:34 | ||||
| chr12:24949489-24949636 | Rare:23 | ||||
| chr12:25195119-25195308 | Common:2; Rare:55 | ||||
| chr12:25250770-25250830 | Rare:9; Clinvar (benign):1 | ||||
| chr12:25958511-25958638 | Rare:44 | ||||
| chr12:25958662-25958814 | Common:2; Rare:52 | ||||
| chr12:25959378-25959529 | Common:1; Rare:25 | ||||
| chr12:26124999-26125293 | Common:2; Rare:64 | ||||
| chr12:26833062-26833405 | Common:3; Rare:100 |