| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62466614-62466911 | Rare:128 | ||||
| chr12:62467020-62467720 | Common:4; Rare:265 | ||||
| chr12:62933200-62933629 | Common:3; Rare:154 | ||||
| chr12:62934842-62935018 | Rare:50 | ||||
| chr12:62934994-62935341 | Common:2; Rare:172 | ||||
| chr12:63779764-63779926 | Common:4; Rare:108; Clinvar (benign):1 | ||||
| chr12:63843590-63844135 | Common:8; Rare:182 | ||||
| chr12:64222227-64222355 | Rare:46 | ||||
| chr12:64404208-64404700 | Common:10; Rare:328 | ||||
| chr12:64404972-64405149 | Rare:35 | ||||
| chr12:64452001-64452195 | Common:2; Rare:139 | ||||
| chr12:64610258-64610546 | Common:9; Rare:193 | ||||
| chr12:64759328-64759534 | Common:2; Rare:122; Clinvar:6 | ||||
| chr12:64780504-64780810 | Common:2; Rare:107 | ||||
| chr12:65169441-65169609 | Common:2; Rare:103; Clinvar:2 |