| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6829637-6829932 | Common:2; Rare:73 | ||||
| chr12:6851227-6851378 | Rare:36 | ||||
| chr12:6851890-6852185 | Rare:75 | ||||
| chr12:6867387-6867677 | Common:2; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868074-6868161 | Common:4; Rare:34 | ||||
| chr12:6870045-6870333 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873274-6873669 | Common:4; Rare:115 | ||||
| chr12:6914483-6914603 | Rare:34 | ||||
| chr12:6946277-6946585 | Common:1; Rare:81 | ||||
| chr12:6967587-6967780 | Rare:54 | ||||
| chr12:6970586-6970988 | Common:4; Rare:128; Clinvar (benign):1 | ||||
| chr12:7018459-7018628 | Common:1; Rare:42 | ||||
| chr12:7060455-7060809 | Rare:67 | ||||
| chr12:7108448-7108696 | Common:1; Rare:71 | ||||
| chr12:7109187-7109280 | Rare:28 |