| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15427478-15427629 | Common:1; Rare:51 | ||||
| chr3:15601524-15601804 | Common:4; Rare:117; Clinvar:1 | ||||
| chr3:16264863-16265227 | Common:2; Rare:123 | ||||
| chr3:16513588-16513817 | Common:4; Rare:53 | ||||
| chr3:19947071-19947457 | Common:6; Rare:143 | ||||
| chr3:20186161-20186347 | Common:1; Rare:51 | ||||
| chr3:23916916-23917196 | Rare:105 | ||||
| chr3:25428107-25428272 | Rare:32 | ||||
| chr3:25783392-25783621 | Common:2; Rare:75; Clinvar (benign):3 | ||||
| chr3:29280991-29281081 | Common:1; Rare:13 | ||||
| chr3:32106425-32106670 | Common:3; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502749-32502910 | Rare:54 | ||||
| chr3:32570680-32570914 | Rare:110 | ||||
| chr3:33277313-33277487 | Common:1; Rare:46 | ||||
| chr3:33798497-33798639 | Common:2; Rare:43 |