| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160565520-160565842 | Common:2; Rare:116 | ||||
| chr3:161105076-161105367 | Common:3; Rare:82 | ||||
| chr3:161221236-161221330 | Rare:30 | ||||
| chr3:167734849-167735229 | Common:3; Rare:121 | ||||
| chr3:168094782-168094890 | Rare:17 | ||||
| chr3:168095088-168095672 | Common:2; Rare:170 | ||||
| chr3:168095836-168095976 | Rare:51 | ||||
| chr3:169773365-169773424 | Rare:19 | ||||
| chr3:170038081-170038245 | Common:3; Rare:37 | ||||
| chr3:170870172-170870278 | Rare:57 | ||||
| chr3:171460263-171460621 | Rare:86 | ||||
| chr3:179148009-179148190 | Common:3; Rare:61 | ||||
| chr3:179604622-179604921 | Common:3; Rare:118 | ||||
| chr3:180602032-180602407 | Common:1; Rare:130 | ||||
| chr3:180989618-180989790 | Rare:76; Clinvar:1; Clinvar (benign):1 |