| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106357696-106357812 | Common:3; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106955463-106955850 | Common:3; Rare:135 | ||||
| chr12:107685706-107685895 | Rare:67 | ||||
| chr12:108561150-108561463 | Common:4; Rare:75 | ||||
| chr12:108562394-108562676 | Common:9; Rare:119; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731450-108731697 | Common:2; Rare:90 | ||||
| chr12:109020971-109021098 | Common:2; Rare:35 | ||||
| chr12:109052460-109052644 | Common:3; Rare:52 | ||||
| chr12:109097867-109098249 | Common:5; Rare:118 | ||||
| chr12:109154557-109154702 | Common:1; Rare:37 | ||||
| chr12:109477287-109477656 | Common:3; Rare:91 | ||||
| chr12:109573448-109573837 | Common:3; Rare:123; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109900002-109900356 | Common:1; Rare:94 | ||||
| chr12:109996294-109996445 | Common:2; Rare:43 | ||||
| chr12:110280973-110281189 | Common:1; Rare:89 |