| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867313-6867532 | Common:2; Rare:82; Clinvar (benign):2 | ||||
| chr12:6873254-6873923 | Common:4; Rare:162 | ||||
| chr12:6904664-6904918 | Common:1; Rare:55 | ||||
| chr12:6914461-6914583 | Rare:38 | ||||
| chr12:6924376-6924561 | Common:1; Rare:41 | ||||
| chr12:6928267-6928667 | Common:3; Rare:122 | ||||
| chr12:6937943-6938343 | Common:1; Rare:179; Clinvar (benign):1 | ||||
| chr12:6943514-6944177 | Common:18; Rare:514; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944453-6944860 | Common:4; Rare:157; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr12:6946321-6946642 | Common:1; Rare:83 | ||||
| chr12:6970514-6970982 | Common:4; Rare:149; Clinvar (benign):1 | ||||
| chr12:7018461-7018729 | Common:1; Rare:73 | ||||
| chr12:7018837-7019054 | Common:3; Rare:52 | ||||
| chr12:7108448-7108695 | Common:1; Rare:71 | ||||
| chr12:7109229-7109379 | Rare:39 |