| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013141-69013334 | Rare:53 | ||||
| chr3:69013584-69013829 | Common:1; Rare:75 | ||||
| chr3:69052133-69052458 | Common:5; Rare:99 | ||||
| chr3:69084754-69085245 | Common:3; Rare:128 | ||||
| chr3:69200500-69200629 | Common:1; Rare:17 | ||||
| chr3:69386076-69386282 | Common:1; Rare:46 | ||||
| chr3:69542567-69542799 | Common:2; Rare:67 | ||||
| chr3:69866059-69866333 | Rare:54; Clinvar (benign):1 | ||||
| chr3:70977641-70978033 | Rare:134; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:71065520-71065820 | Common:1; Rare:56 | ||||
| chr3:71130505-71130674 | Rare:61; Clinvar:2 | ||||
| chr3:71130740-71130956 | Rare:39 | ||||
| chr3:71581832-71582403 | Common:1; Rare:152 | ||||
| chr3:72996688-72997061 | Common:2; Rare:137 | ||||
| chr3:73624102-73624477 | Common:6; Rare:117 |