| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107761065-107761367 | Common:6; Rare:113 | ||||
| chr12:108515054-108515319 | Common:1; Rare:79 | ||||
| chr12:108561098-108561481 | Common:4; Rare:105 | ||||
| chr12:108562388-108562726 | Common:9; Rare:139; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108730358-108730471 | Rare:29 | ||||
| chr12:108731433-108731706 | Common:2; Rare:99 | ||||
| chr12:108857559-108857850 | Common:3; Rare:139 | ||||
| chr12:109020981-109021144 | Common:3; Rare:48 | ||||
| chr12:109052470-109052659 | Common:3; Rare:55 | ||||
| chr12:109097442-109097623 | Rare:62; Clinvar:1 | ||||
| chr12:109440844-109441147 | Common:1; Rare:64 | ||||
| chr12:109477260-109477679 | Common:3; Rare:116 | ||||
| chr12:109573421-109573866 | Common:5; Rare:149; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880678 | Common:1; Rare:93 | ||||
| chr12:109900174-109900360 | Rare:64 |