| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6688867-6689081 | Rare:68 | ||||
| chr12:6689459-6689756 | Common:2; Rare:76 | ||||
| chr12:6723970-6724158 | Rare:45 | ||||
| chr12:6752937-6753189 | Common:6; Rare:77 | ||||
| chr12:6851922-6852182 | Rare:66 | ||||
| chr12:6867381-6867611 | Common:2; Rare:116; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873291-6873534 | Common:1; Rare:72 | ||||
| chr12:6914401-6914618 | Rare:57 | ||||
| chr12:6943517-6943817 | Common:4; Rare:125 | ||||
| chr12:6943999-6944172 | Common:2; Rare:163; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970612-6970976 | Common:4; Rare:116; Clinvar (benign):1 | ||||
| chr12:7108448-7108712 | Common:1; Rare:73 | ||||
| chr12:7108923-7109276 | Common:13; Rare:108 | ||||
| chr12:7189519-7189731 | Rare:72; Clinvar:4 | ||||
| chr12:7502716-7502755 | Rare:9 |