| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:70977641-70978031 | Rare:134; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:71130508-71130685 | Rare:69; Clinvar:2 | ||||
| chr3:71245035-71245145 | Rare:25 | ||||
| chr3:71581882-71582392 | Common:1; Rare:139 | ||||
| chr3:71754767-71754899 | Rare:38 | ||||
| chr3:73624133-73624454 | Common:6; Rare:100 | ||||
| chr3:81761612-81761794 | Common:3; Rare:63; Clinvar:1 | ||||
| chr3:87227186-87227477 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058878-88059304 | Common:4; Rare:164 | ||||
| chr3:88149605-88149758 | Common:1; Rare:35 | ||||
| chr3:88149856-88150043 | Common:5; Rare:75 | ||||
| chr3:94062897-94063069 | Rare:44 | ||||
| chr3:97764448-97764802 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821921-97822113 | Rare:69 | ||||
| chr3:98732444-98732532 | Rare:15 |