| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49366781-49367021 | Common:1; Rare:60 | ||||
| chr12:49367212-49367573 | Common:1; Rare:97 | ||||
| chr12:49568104-49568419 | Common:2; Rare:74 | ||||
| chr12:49828402-49828539 | Rare:49 | ||||
| chr12:50085043-50085364 | Common:1; Rare:84 | ||||
| chr12:50167303-50167699 | Common:2; Rare:105 | ||||
| chr12:50283477-50283656 | Common:1; Rare:58 | ||||
| chr12:51026319-51026510 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51238756-51238901 | Rare:66 | ||||
| chr12:51270276-51270483 | Common:3; Rare:55 | ||||
| chr12:51391397-51391460 | Common:1; Rare:13 | ||||
| chr12:51391592-51391737 | Common:1; Rare:43 | ||||
| chr12:51912210-51912442 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr12:52949789-52950071 | Rare:59 | ||||
| chr12:53006363-53006486 | Common:1; Rare:54 |