| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:168249932-168250042 | Rare:21 | ||||
| chr3:168250575-168250785 | Common:1; Rare:33 | ||||
| chr3:169764296-169764665 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:169764783-169765219 | Common:1; Rare:155; Clinvar:22; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr3:169771867-169771917 | Rare:12 | ||||
| chr3:169772001-169772274 | Common:3; Rare:127 | ||||
| chr3:169814000-169814097 | Common:1; Rare:20 | ||||
| chr3:169932131-169932513 | Common:2; Rare:87 | ||||
| chr3:169945435-169945550 | Rare:25 | ||||
| chr3:169965651-169965794 | Common:1; Rare:27 | ||||
| chr3:169965807-169966055 | Common:1; Rare:43 | ||||
| chr3:170044917-170045199 | Common:3; Rare:44 | ||||
| chr3:170055483-170055747 | Common:3; Rare:46 | ||||
| chr3:170180993-170181076 | Rare:21 | ||||
| chr3:170355678-170355941 | Common:1; Rare:56 |