| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734804-167735209 | Common:3; Rare:131; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735609-167735731 | Rare:28 | ||||
| chr3:169146496-169146539 | Rare:24 | ||||
| chr3:169773331-169773424 | Rare:29 | ||||
| chr3:169812902-169812944 | Rare:5 | ||||
| chr3:169966725-169966858 | Rare:58 | ||||
| chr3:170222372-170222553 | Common:1; Rare:61 | ||||
| chr3:170357371-170357784 | Common:3; Rare:180 | ||||
| chr3:170870163-170870250 | Rare:52 | ||||
| chr3:170908578-170908806 | Common:1; Rare:62 | ||||
| chr3:172039459-172039656 | Common:1; Rare:65 | ||||
| chr3:172710989-172711387 | Common:2; Rare:117 | ||||
| chr3:172750356-172750789 | Common:4; Rare:97 | ||||
| chr3:177197129-177197396 | Rare:90 | ||||
| chr3:179347605-179347774 | Common:1; Rare:40 |