| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:389262-389377 | Rare:43 | ||||
| chr12:401436-401647 | Rare:59 | ||||
| chr12:643624-643660 | Rare:6 | ||||
| chr12:752327-752602 | Common:1; Rare:78 | ||||
| chr12:991101-991322 | Common:3; Rare:100 | ||||
| chr12:1970724-1970856 | Common:1; Rare:25 | ||||
| chr12:2004427-2004511 | Rare:29 | ||||
| chr12:2812542-2812713 | Common:1; Rare:45 | ||||
| chr12:2877031-2877253 | Rare:67 | ||||
| chr12:2959843-2959944 | Common:1; Rare:26 | ||||
| chr12:3077246-3077453 | Common:7; Rare:86 | ||||
| chr12:4275444-4275590 | Common:2; Rare:22 | ||||
| chr12:4320941-4321266 | Common:5; Rare:126 | ||||
| chr12:4538457-4538798 | Rare:67 | ||||
| chr12:4649041-4649178 | Common:1; Rare:53; Clinvar (benign):2 |