| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134224533-134224690 | Rare:58 | ||||
| chr11:134253314-134253608 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389249-389360 | Rare:39 | ||||
| chr12:401436-401669 | Rare:65 | ||||
| chr12:610367-610510 | Common:1; Rare:15 | ||||
| chr12:643582-643859 | Common:2; Rare:56 | ||||
| chr12:752306-752605 | Common:1; Rare:89 | ||||
| chr12:949626-949844 | Common:4; Rare:66 | ||||
| chr12:991101-991289 | Common:2; Rare:84 | ||||
| chr12:2877045-2877262 | Rare:65 | ||||
| chr12:2959821-2959973 | Common:1; Rare:39 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538444-4538807 | Rare:75 | ||||
| chr12:4649045-4649171 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr12:6124528-6124762 | Rare:32; Clinvar:1 |