| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:62318890-62319049 | Rare:67 | ||||
| chr3:63863777-63864135 | Common:7; Rare:120 | ||||
| chr3:67654582-67654727 | Common:1; Rare:51 | ||||
| chr3:69013652-69013756 | Rare:27 | ||||
| chr3:69052249-69052351 | Common:2; Rare:44 | ||||
| chr3:69084853-69085044 | Common:3; Rare:53 | ||||
| chr3:81761634-81761702 | Rare:23 | ||||
| chr3:87226988-87227334 | Common:1; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058953-88059242 | Common:2; Rare:89 | ||||
| chr3:94062904-94063011 | Rare:34 | ||||
| chr3:99817568-99817915 | Rare:101 | ||||
| chr3:100401407-100401576 | Common:1; Rare:29 | ||||
| chr3:101513136-101513319 | Common:8; Rare:36 | ||||
| chr3:101561746-101561910 | Common:1; Rare:58 | ||||
| chr3:101686670-101686841 | Common:2; Rare:76 |