| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160423491-160423858 | Rare:103 | ||||
| chr3:160515187-160515577 | Common:1; Rare:74 | ||||
| chr3:160568106-160568375 | Common:1; Rare:61 | ||||
| chr3:165496276-165496526 | Common:1; Rare:36 | ||||
| chr3:167695593-167695857 | Rare:68; Clinvar (pathogenic):1 | ||||
| chr3:168010552-168010750 | Common:1; Rare:50 | ||||
| chr3:169765015-169765189 | Rare:84; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr3:170270601-170270687 | Common:2; Rare:15 | ||||
| chr3:170367614-170367846 | Common:2; Rare:35 | ||||
| chr3:172129910-172130009 | Common:1; Rare:15 | ||||
| chr3:172169023-172169280 | Common:4; Rare:40 | ||||
| chr3:172218024-172218314 | Rare:32 | ||||
| chr3:172393932-172394052 | Common:2; Rare:17 | ||||
| chr3:172760223-172760291 | Rare:17 | ||||
| chr3:177026329-177026513 | Rare:39; Clinvar:1; Clinvar (benign):1 |