| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335621-46335770 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762476-46762676 | Common:3; Rare:76 | ||||
| chr22:50244973-50245067 | Common:1; Rare:38 | ||||
| chr22:50525547-50525742 | Common:4; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50628093-50628282 | Common:9; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783859 | Common:2; Rare:87 | ||||
| chr3:196676-197334 | Common:5; Rare:217 | ||||
| chr3:2098627-2098962 | Common:4; Rare:133 | ||||
| chr3:3126813-3126990 | Common:4; Rare:78; Clinvar (benign):2 | ||||
| chr3:4303253-4303412 | Common:1; Rare:62 | ||||
| chr3:4467267-4467350 | Rare:30; Clinvar:1 | ||||
| chr3:4493151-4493537 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:8501620-8501962 | Common:2; Rare:126 | ||||
| chr3:8644781-8644906 | Common:2; Rare:33 | ||||
| chr3:9249549-9249750 | Common:1; Rare:43 |