| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6959078-6959358 | Common:1; Rare:54 | ||||
| chr12:6970486-6970993 | Common:4; Rare:161; Clinvar (benign):1 | ||||
| chr12:7018364-7018678 | Common:2; Rare:90 | ||||
| chr12:7018745-7019050 | Common:4; Rare:81 | ||||
| chr12:7107822-7108076 | Rare:39 | ||||
| chr12:7108345-7108712 | Common:2; Rare:110 | ||||
| chr12:7109182-7109385 | Rare:53 | ||||
| chr12:7189498-7189761 | Common:1; Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:7369314-7369628 | Rare:92 | ||||
| chr12:7936090-7936443 | Common:4; Rare:54 | ||||
| chr12:8032532-8032802 | Common:5; Rare:82 | ||||
| chr12:8032900-8032991 | Common:2; Rare:17 | ||||
| chr12:8081854-8081968 | Common:1; Rare:24 | ||||
| chr12:8081982-8082421 | Common:2; Rare:133; Clinvar:1 | ||||
| chr12:8227596-8227712 | Rare:34 |