| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:166634396-166634634 | Common:3; Rare:38 | ||||
| chr3:169232945-169233229 | Common:5; Rare:53 | ||||
| chr3:169239875-169239958 | Common:1; Rare:16 | ||||
| chr3:169241692-169241826 | Rare:21 | ||||
| chr3:169242002-169242152 | Common:1; Rare:26 | ||||
| chr3:169242254-169242572 | Rare:65 | ||||
| chr3:169764286-169764653 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:169764976-169765308 | Common:1; Rare:117; Clinvar:7; Clinvar (pathogenic):5 | ||||
| chr3:169769140-169769326 | Common:2; Rare:29 | ||||
| chr3:169769335-169769392 | Rare:27 | ||||
| chr3:169771865-169771988 | Common:2; Rare:26 | ||||
| chr3:169772027-169772249 | Common:3; Rare:94 | ||||
| chr3:169811661-169811922 | Common:3; Rare:44 | ||||
| chr3:169891968-169892086 | Common:3; Rare:27 | ||||
| chr3:170111479-170111790 | Common:1; Rare:56 |