| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169812902-169813080 | Common:2; Rare:33 | ||||
| chr3:169966706-169966833 | Rare:53 | ||||
| chr3:170870168-170870308 | Rare:69 | ||||
| chr3:170908578-170908857 | Common:1; Rare:80 | ||||
| chr3:171771341-171771485 | Common:1; Rare:26 | ||||
| chr3:173397475-173397825 | Common:4; Rare:116 | ||||
| chr3:177197142-177197377 | Rare:81 | ||||
| chr3:179451367-179451694 | Common:1; Rare:116 | ||||
| chr3:179562665-179563028 | Rare:119 | ||||
| chr3:179604610-179604857 | Common:2; Rare:94 | ||||
| chr3:180601986-180602249 | Common:1; Rare:86 | ||||
| chr3:180912391-180912713 | Common:2; Rare:111 | ||||
| chr3:180989618-180989782 | Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711677-181711974 | Rare:88 | ||||
| chr3:182793393-182793630 | Common:3; Rare:53 |