| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63150466-63150778 | Common:1; Rare:112 | ||||
| chr12:63150894-63151028 | Common:1; Rare:34 | ||||
| chr12:63151031-63151044 | Rare:3 | ||||
| chr12:63151105-63151326 | Common:1; Rare:41 | ||||
| chr12:63779729-63779871 | Common:2; Rare:51 | ||||
| chr12:64222080-64222349 | Rare:84 | ||||
| chr12:64404232-64404645 | Common:5; Rare:149 | ||||
| chr12:64452036-64452182 | Common:1; Rare:55 | ||||
| chr12:64759182-64759479 | Rare:91; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169532-65169602 | Rare:28; Clinvar:1 | ||||
| chr12:66130703-66130876 | Rare:58 | ||||
| chr12:67269139-67269386 | Common:2; Rare:70 | ||||
| chr12:67648596-67648757 | Rare:42 | ||||
| chr12:68332273-68332631 | Common:1; Rare:115 | ||||
| chr12:68610695-68611028 | Common:1; Rare:145 |