| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108561150-108561431 | Common:3; Rare:67 | ||||
| chr12:108562394-108562658 | Common:8; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:108857581-108857865 | Common:3; Rare:125 | ||||
| chr12:109116420-109116648 | Rare:38 | ||||
| chr12:109131270-109131390 | Rare:23 | ||||
| chr12:109154568-109154686 | Common:1; Rare:32 | ||||
| chr12:109477275-109477656 | Common:3; Rare:97 | ||||
| chr12:109573430-109573853 | Common:3; Rare:137; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880668 | Common:1; Rare:91 | ||||
| chr12:109900189-109900349 | Rare:63 | ||||
| chr12:109996220-109996454 | Common:2; Rare:67 | ||||
| chr12:109999103-109999211 | Rare:16 | ||||
| chr12:110124133-110124466 | Common:2; Rare:107 | ||||
| chr12:110124632-110124767 | Common:2; Rare:24 | ||||
| chr12:110124772-110124813 | Rare:8 |