| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53321204-53321419 | Common:2; Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53321580-53321717 | Common:1; Rare:28; Clinvar:1 | ||||
| chr12:53324850-53325038 | Common:1; Rare:47 | ||||
| chr12:53344794-53344928 | Rare:31 | ||||
| chr12:53380562-53380962 | Common:2; Rare:216 | ||||
| chr12:53441455-53441787 | Common:1; Rare:95 | ||||
| chr12:53451781-53452110 | Rare:78 | ||||
| chr12:53452434-53452834 | Common:4; Rare:252 | ||||
| chr12:53492972-53493285 | Common:3; Rare:84 | ||||
| chr12:53499449-53499565 | Rare:28 | ||||
| chr12:53500662-53500968 | Common:3; Rare:67 | ||||
| chr12:53501208-53501375 | Rare:40 | ||||
| chr12:53625871-53626188 | Common:1; Rare:75 | ||||
| chr12:53626322-53626617 | Common:3; Rare:66 | ||||
| chr12:53676033-53676370 | Common:3; Rare:163 |