| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:161371662-161371916 | Common:1; Rare:39 | ||||
| chr3:161371926-161372063 | Rare:36 | ||||
| chr3:167734839-167735266 | Common:5; Rare:134; Clinvar (benign):1 | ||||
| chr3:169773307-169773424 | Rare:40 | ||||
| chr3:169812896-169813068 | Common:2; Rare:30 | ||||
| chr3:169966545-169966858 | Common:2; Rare:103 | ||||
| chr3:170222287-170222699 | Common:4; Rare:143 | ||||
| chr3:170358195-170358511 | Common:4; Rare:105 | ||||
| chr3:170870158-170870359 | Rare:94 | ||||
| chr3:170908591-170908806 | Common:1; Rare:59 | ||||
| chr3:172039435-172039671 | Common:1; Rare:75 | ||||
| chr3:172750533-172750803 | Common:3; Rare:79 | ||||
| chr3:173397436-173397814 | Common:4; Rare:122 | ||||
| chr3:177196387-177196550 | Rare:43 | ||||
| chr3:179604610-179604877 | Common:2; Rare:104 |