| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170870163-170870304 | Rare:74 | ||||
| chr3:170908578-170908845 | Common:1; Rare:75 | ||||
| chr3:171026654-171026841 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:172039494-172039698 | Common:1; Rare:72 | ||||
| chr3:172040397-172040587 | Common:1; Rare:46 | ||||
| chr3:172711063-172711350 | Common:1; Rare:72 | ||||
| chr3:172750556-172750794 | Common:3; Rare:69 | ||||
| chr3:179576433-179576718 | Common:2; Rare:54 | ||||
| chr3:179604614-179604915 | Common:2; Rare:120 | ||||
| chr3:180602050-180602258 | Common:1; Rare:73 | ||||
| chr3:180989618-180989842 | Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793405-182793667 | Common:3; Rare:59 | ||||
| chr3:183099406-183099742 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253039-183253309 | Common:3; Rare:78 | ||||
| chr3:183635595-183635745 | Common:2; Rare:40 |