| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76348125-76348195 | Rare:24 | ||||
| chr12:76348297-76348694 | Common:2; Rare:128; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:76558904-76559185 | Common:2; Rare:55 | ||||
| chr12:76559450-76560054 | Common:4; Rare:184 | ||||
| chr12:76763820-76764352 | Common:5; Rare:215 | ||||
| chr12:76878990-76879217 | Rare:76 | ||||
| chr12:77065205-77065230 | Rare:3 | ||||
| chr12:77065469-77065653 | Common:1; Rare:64 | ||||
| chr12:77065985-77066165 | Rare:43 | ||||
| chr12:79689492-79689637 | Common:1; Rare:38 | ||||
| chr12:79689773-79690013 | Common:1; Rare:80 | ||||
| chr12:79690167-79690233 | Rare:21 | ||||
| chr12:79690234-79690272 | Rare:8 | ||||
| chr12:79690369-79690760 | Common:2; Rare:110 | ||||
| chr12:79690949-79691189 | Rare:71 |