| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851227-6851489 | Rare:63 | ||||
| chr12:6851876-6852180 | Rare:81 | ||||
| chr12:6867381-6867615 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6870046-6870450 | Common:1; Rare:134; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6873280-6873541 | Common:2; Rare:75 | ||||
| chr12:6904687-6904890 | Rare:45 | ||||
| chr12:6914457-6914562 | Rare:31 | ||||
| chr12:6943537-6943825 | Common:3; Rare:120 | ||||
| chr12:6943857-6944173 | Common:14; Rare:333; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970594-6970988 | Common:4; Rare:125; Clinvar (benign):1 | ||||
| chr12:7018440-7018580 | Common:1; Rare:42 | ||||
| chr12:7189551-7189733 | Rare:67; Clinvar:4 | ||||
| chr12:7936149-7936465 | Common:4; Rare:52 | ||||
| chr12:8032590-8032759 | Rare:61 | ||||
| chr12:8697731-8698043 | Common:1; Rare:123 |