| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159763170-159763348 | Rare:32 | ||||
| chr3:159852997-159853274 | Rare:49 | ||||
| chr3:160399177-160399355 | Rare:53; Clinvar:3 | ||||
| chr3:160399498-160399670 | Rare:44; Clinvar:1 | ||||
| chr3:160449535-160449642 | Rare:18 | ||||
| chr3:160449743-160450027 | Common:2; Rare:90 | ||||
| chr3:160565541-160565842 | Common:2; Rare:105 | ||||
| chr3:160677031-160677226 | Common:3; Rare:29 | ||||
| chr3:160755469-160755635 | Common:1; Rare:57 | ||||
| chr3:161105243-161105372 | Common:2; Rare:45 | ||||
| chr3:161371466-161371527 | Common:2; Rare:11 | ||||
| chr3:161371543-161371846 | Common:1; Rare:47 | ||||
| chr3:167734807-167735254 | Common:5; Rare:145; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735607-167735763 | Rare:39 | ||||
| chr3:169663379-169663459 | Common:1; Rare:20 |