| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399196-160399290 | Rare:22; Clinvar:1 | ||||
| chr3:160399517-160399687 | Rare:38 | ||||
| chr3:160449743-160450040 | Common:2; Rare:97 | ||||
| chr3:160565250-160565814 | Common:3; Rare:190 | ||||
| chr3:160566083-160566397 | Rare:56 | ||||
| chr3:161105032-161105380 | Common:4; Rare:102 | ||||
| chr3:167734810-167735252 | Common:5; Rare:144; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:168095898-168096250 | Common:1; Rare:117 | ||||
| chr3:169663379-169663786 | Common:2; Rare:98 | ||||
| chr3:169773242-169773418 | Rare:58 | ||||
| chr3:169812673-169812991 | Common:1; Rare:53 | ||||
| chr3:170421137-170421313 | Common:2; Rare:34 | ||||
| chr3:170870157-170870282 | Rare:73 | ||||
| chr3:171809774-171809889 | Rare:32 | ||||
| chr3:172039461-172039683 | Common:1; Rare:77 |