| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158801821-158802162 | Common:3; Rare:118 | ||||
| chr3:160399520-160399669 | Rare:30 | ||||
| chr3:160565442-160565868 | Common:2; Rare:152 | ||||
| chr3:167734832-167735071 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773242-169773421 | Rare:60 | ||||
| chr3:169975477-169975716 | Common:1; Rare:37 | ||||
| chr3:170037717-170038141 | Common:7; Rare:102 | ||||
| chr3:172039647-172039767 | Common:1; Rare:30 | ||||
| chr3:172040487-172040616 | Rare:24 | ||||
| chr3:177027070-177027348 | Rare:51 | ||||
| chr3:179147962-179148172 | Common:2; Rare:62 | ||||
| chr3:179562669-179562993 | Rare:105 | ||||
| chr3:179604632-179604807 | Common:1; Rare:51 | ||||
| chr3:183099583-183099742 | Common:1; Rare:35 | ||||
| chr3:183253119-183253293 | Common:2; Rare:52 |