| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6868653-6868986 | Common:2; Rare:91; Clinvar (pathogenic):1 | ||||
| chr12:6869430-6869773 | Common:1; Rare:96; Clinvar (pathogenic):1 | ||||
| chr12:6870045-6870288 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873274-6873546 | Common:2; Rare:79 | ||||
| chr12:6927559-6927845 | Rare:75 | ||||
| chr12:6943531-6943834 | Common:4; Rare:135 | ||||
| chr12:6943900-6944161 | Common:10; Rare:263; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946347-6946644 | Common:1; Rare:76 | ||||
| chr12:6951268-6951399 | Rare:37 | ||||
| chr12:6967498-6967640 | Rare:54 | ||||
| chr12:6967895-6968144 | Rare:51 | ||||
| chr12:6970446-6970969 | Common:4; Rare:161; Clinvar (benign):1 | ||||
| chr12:7018431-7018732 | Common:1; Rare:88 | ||||
| chr12:7108475-7108696 | Common:1; Rare:61 | ||||
| chr12:7109105-7109329 | Rare:70 |