| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867361-6867625 | Common:2; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868074-6868161 | Common:4; Rare:34 | ||||
| chr12:6873334-6873541 | Common:1; Rare:55 | ||||
| chr12:6904665-6904880 | Rare:49 | ||||
| chr12:6914400-6914564 | Rare:41 | ||||
| chr12:6937944-6938227 | Common:1; Rare:123; Clinvar (benign):1 | ||||
| chr12:6943531-6943826 | Common:4; Rare:126 | ||||
| chr12:6943842-6944166 | Common:14; Rare:346; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6959195-6959340 | Rare:28 | ||||
| chr12:6970607-6970977 | Common:4; Rare:117; Clinvar (benign):1 | ||||
| chr12:7130256-7130401 | Common:4; Rare:39 | ||||
| chr12:7189549-7189735 | Rare:67; Clinvar:4 | ||||
| chr12:8032562-8032738 | Common:4; Rare:61 | ||||
| chr12:8697257-8697326 | Common:1; Rare:11 | ||||
| chr12:8697740-8698049 | Common:1; Rare:123 |