| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723956-6724177 | Rare:59 | ||||
| chr12:6724196-6724303 | Common:1; Rare:24 | ||||
| chr12:6752927-6753191 | Common:6; Rare:80 | ||||
| chr12:6851236-6851472 | Rare:56 | ||||
| chr12:6851922-6852271 | Common:1; Rare:85 | ||||
| chr12:6863551-6863885 | Common:1; Rare:74 | ||||
| chr12:6867406-6867615 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868861-6869181 | Rare:98; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:6869465-6869773 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
| chr12:6873282-6873534 | Common:2; Rare:73 | ||||
| chr12:6943721-6944172 | Common:17; Rare:428; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946347-6946585 | Common:1; Rare:62 | ||||
| chr12:6970208-6970983 | Common:5; Rare:259; Clinvar (benign):1 | ||||
| chr12:7108468-7108683 | Common:1; Rare:62 | ||||
| chr12:7109125-7109276 | Rare:51 |