| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:161221226-161221389 | Common:2; Rare:53 | ||||
| chr3:161371518-161371728 | Common:2; Rare:36 | ||||
| chr3:161372842-161372961 | Rare:22 | ||||
| chr3:165196397-165196497 | Common:1; Rare:26 | ||||
| chr3:167734837-167735266 | Common:5; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735602-167735790 | Rare:53; Clinvar:1 | ||||
| chr3:169147539-169147879 | Common:5; Rare:76 | ||||
| chr3:169663560-169663778 | Common:1; Rare:46 | ||||
| chr3:169772748-169772831 | Rare:20 | ||||
| chr3:169773331-169773424 | Rare:29 | ||||
| chr3:169812478-169812777 | Common:2; Rare:72 | ||||
| chr3:169966711-169966851 | Rare:60 | ||||
| chr3:170870167-170870286 | Rare:64 | ||||
| chr3:170908580-170908844 | Common:1; Rare:74 | ||||
| chr3:171460107-171460496 | Common:2; Rare:85 |