| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:62318894-62319068 | Rare:71 | ||||
| chr3:63863740-63864189 | Common:8; Rare:146 | ||||
| chr3:63911996-63912116 | Rare:40 | ||||
| chr3:66038464-66038656 | Rare:42 | ||||
| chr3:66038744-66039065 | Common:3; Rare:116 | ||||
| chr3:67654557-67654809 | Common:2; Rare:97 | ||||
| chr3:69013590-69013756 | Rare:44 | ||||
| chr3:69080342-69080446 | Rare:45 | ||||
| chr3:69084796-69085063 | Common:3; Rare:74 | ||||
| chr3:69200491-69200614 | Rare:18 | ||||
| chr3:70977641-70977934 | Rare:98; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:71130539-71130692 | Common:1; Rare:61; Clinvar:2 | ||||
| chr3:71581882-71582096 | Common:1; Rare:46 | ||||
| chr3:71582133-71582392 | Rare:80 | ||||
| chr3:72996715-72997030 | Common:2; Rare:117 |