| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10167660-10167930 | Common:4; Rare:46 | ||||
| chr12:10172016-10172268 | Rare:65 | ||||
| chr12:10409408-10409663 | Common:4; Rare:70 | ||||
| chr12:10613508-10613686 | Common:1; Rare:70 | ||||
| chr12:11171092-11171243 | Rare:55 | ||||
| chr12:11171545-11171790 | Common:6; Rare:78 | ||||
| chr12:12356999-12357187 | Common:4; Rare:101 | ||||
| chr12:12611808-12612088 | Common:1; Rare:81 | ||||
| chr12:12696634-12696734 | Rare:32 | ||||
| chr12:12717204-12717486 | Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717678-12717728 | Rare:12; Clinvar (benign):1 | ||||
| chr12:12725616-12725929 | Common:3; Rare:69 | ||||
| chr12:12891318-12891567 | Common:1; Rare:48 | ||||
| chr12:12989276-12989566 | Rare:81 | ||||
| chr12:13000204-13000468 | Common:2; Rare:89 |