| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63863771-63864110 | Common:7; Rare:113 | ||||
| chr3:64013439-64013720 | Common:2; Rare:86 | ||||
| chr3:66038470-66038657 | Rare:43 | ||||
| chr3:67654552-67654805 | Common:2; Rare:100 | ||||
| chr3:69013590-69013993 | Common:2; Rare:134 | ||||
| chr3:71130539-71130664 | Rare:47; Clinvar:2 | ||||
| chr3:81761413-81761735 | Common:8; Rare:126; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:81761738-81761873 | Rare:35 | ||||
| chr3:87227032-87227482 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058932-88059294 | Common:3; Rare:133 | ||||
| chr3:88149613-88150044 | Common:6; Rare:131 | ||||
| chr3:93973628-93973994 | Rare:122; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:94062867-94063091 | Rare:58 | ||||
| chr3:97764439-97764796 | Common:1; Rare:82; Clinvar (benign):1 | ||||
| chr3:97821921-97822101 | Rare:65 |