| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568249-6568393 | Rare:55 | ||||
| chr12:6689417-6689769 | Common:2; Rare:94 | ||||
| chr12:6723970-6724163 | Rare:50 | ||||
| chr12:6724220-6724296 | Rare:13 | ||||
| chr12:6752944-6753189 | Common:6; Rare:77 | ||||
| chr12:6851924-6852174 | Rare:63 | ||||
| chr12:6867365-6867680 | Common:2; Rare:147; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869130-6869380 | Rare:81; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6873280-6873554 | Common:2; Rare:79 | ||||
| chr12:6970616-6970961 | Common:3; Rare:108 | ||||
| chr12:7018431-7018580 | Common:1; Rare:46 | ||||
| chr12:7090197-7090480 | Common:5; Rare:61; Clinvar:1 | ||||
| chr12:7091872-7091982 | Rare:28 | ||||
| chr12:7108410-7108695 | Common:1; Rare:86 | ||||
| chr12:7108923-7108959 | Rare:2 |