| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112109381-112109566 | Common:1; Rare:37 | ||||
| chr12:112125321-112125633 | Rare:75 | ||||
| chr12:112382369-112382617 | Common:1; Rare:79 | ||||
| chr12:112409138-112409324 | Common:1; Rare:43 | ||||
| chr12:112409483-112409718 | Common:1; Rare:77 | ||||
| chr12:112418570-112419003 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:112419105-112419365 | Common:2; Rare:61; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:112906825-112907023 | Rare:39 | ||||
| chr12:112907092-112907222 | Rare:44 | ||||
| chr12:112937732-112938052 | Common:1; Rare:38 | ||||
| chr12:112938295-112938589 | Common:4; Rare:68 | ||||
| chr12:112978095-112978622 | Common:1; Rare:99 | ||||
| chr12:113089522-113089565 | Common:1; Rare:5 | ||||
| chr12:113184708-113185142 | Common:2; Rare:111 | ||||
| chr12:113185284-113185807 | Common:10; Rare:201 |