| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734825-167735071 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773307-169773415 | Rare:36 | ||||
| chr3:170870168-170870286 | Rare:63 | ||||
| chr3:171460773-171460955 | Rare:44 | ||||
| chr3:172040349-172040587 | Common:2; Rare:67 | ||||
| chr3:174440809-174441006 | Common:2; Rare:54 | ||||
| chr3:177196465-177196606 | Rare:49 | ||||
| chr3:178536120-178536463 | Common:3; Rare:58 | ||||
| chr3:179604614-179604846 | Common:2; Rare:84 | ||||
| chr3:180602100-180602269 | Common:1; Rare:59 | ||||
| chr3:180912621-180912713 | Common:1; Rare:34 | ||||
| chr3:180989652-180989790 | Rare:60; Clinvar:1 | ||||
| chr3:184017868-184018059 | Rare:54 | ||||
| chr3:184135209-184135413 | Common:2; Rare:62; Clinvar:5 | ||||
| chr3:184249540-184249682 | Rare:40 |