| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169966170-169966542 | Common:1; Rare:66 | ||||
| chr3:169966677-169967088 | Common:5; Rare:134 | ||||
| chr3:170870163-170870280 | Rare:66 | ||||
| chr3:170908578-170908845 | Common:1; Rare:75 | ||||
| chr3:171026656-171026996 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:171460258-171460592 | Rare:80 | ||||
| chr3:172039494-172039683 | Common:1; Rare:65 | ||||
| chr3:172711038-172711196 | Rare:67 | ||||
| chr3:174440669-174440971 | Common:2; Rare:82 | ||||
| chr3:177196465-177196773 | Common:2; Rare:102 | ||||
| chr3:179148028-179148152 | Common:1; Rare:31 | ||||
| chr3:179604610-179604921 | Common:3; Rare:124 | ||||
| chr3:180602111-180602269 | Common:1; Rare:58 | ||||
| chr3:180912336-180912482 | Common:3; Rare:36 | ||||
| chr3:180989610-180989843 | Rare:98; Clinvar:1; Clinvar (benign):1 |