| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6829644-6829774 | Common:1; Rare:23 | ||||
| chr12:6851236-6851497 | Rare:62 | ||||
| chr12:6851873-6852174 | Rare:80 | ||||
| chr12:6867364-6867615 | Common:2; Rare:123; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868054-6868161 | Common:4; Rare:45 | ||||
| chr12:6869578-6869773 | Rare:69; Clinvar (pathogenic):1 | ||||
| chr12:6873282-6873697 | Common:4; Rare:115 | ||||
| chr12:6904676-6904910 | Rare:52 | ||||
| chr12:6937956-6938261 | Common:1; Rare:121; Clinvar (benign):1 | ||||
| chr12:6943516-6943864 | Common:6; Rare:183 | ||||
| chr12:6943921-6944172 | Common:9; Rare:250; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6967587-6967728 | Rare:43 | ||||
| chr12:6970586-6970988 | Common:4; Rare:128; Clinvar (benign):1 | ||||
| chr12:7018431-7018580 | Common:1; Rare:46 | ||||
| chr12:7018830-7019029 | Common:1; Rare:49 |