| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160755922-160756265 | Common:1; Rare:88 | ||||
| chr3:161105075-161105360 | Common:3; Rare:83 | ||||
| chr3:161221245-161221360 | Common:2; Rare:41 | ||||
| chr3:161221426-161221582 | Common:2; Rare:40 | ||||
| chr3:167734804-167735257 | Common:5; Rare:149; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735615-167735752 | Rare:34 | ||||
| chr3:169772767-169772821 | Rare:12 | ||||
| chr3:169773323-169773425 | Rare:33 | ||||
| chr3:169812902-169813053 | Common:2; Rare:25 | ||||
| chr3:169966706-169966870 | Rare:67 | ||||
| chr3:170870163-170870254 | Rare:53 | ||||
| chr3:170908583-170908827 | Common:1; Rare:68 | ||||
| chr3:171771228-171771491 | Common:2; Rare:52 | ||||
| chr3:172039435-172039714 | Common:2; Rare:90 | ||||
| chr3:172039756-172039771 | Rare:4 |