| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108730413-108730457 | Rare:10 | ||||
| chr12:108730686-108730836 | Rare:31 | ||||
| chr12:108731453-108731696 | Common:2; Rare:88 | ||||
| chr12:108857525-108857822 | Common:2; Rare:147 | ||||
| chr12:109093399-109093754 | Common:3; Rare:118 | ||||
| chr12:109098128-109098575 | Common:2; Rare:182; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:109116418-109116674 | Rare:43 | ||||
| chr12:109130979-109131512 | Common:2; Rare:97 | ||||
| chr12:109131854-109131990 | Common:1; Rare:36 | ||||
| chr12:109154557-109154832 | Common:3; Rare:63 | ||||
| chr12:109477275-109477664 | Common:3; Rare:101 | ||||
| chr12:109573430-109573813 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109900159-109900356 | Rare:67 | ||||
| chr12:110450253-110450401 | Common:2; Rare:58 | ||||
| chr12:110502058-110502332 | Common:1; Rare:100 |