| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160755449-160755666 | Common:1; Rare:82 | ||||
| chr3:160756155-160756482 | Rare:85 | ||||
| chr3:161105071-161105355 | Common:3; Rare:83 | ||||
| chr3:161221048-161221362 | Common:3; Rare:93 | ||||
| chr3:161371437-161371590 | Common:2; Rare:29 | ||||
| chr3:161371870-161372188 | Rare:67 | ||||
| chr3:167734837-167735205 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735593-167735721 | Rare:33 | ||||
| chr3:169773331-169773424 | Rare:29 | ||||
| chr3:169966706-169966858 | Rare:65 | ||||
| chr3:170870160-170870379 | Rare:92 | ||||
| chr3:170908584-170908845 | Common:1; Rare:73 | ||||
| chr3:179147998-179148196 | Common:3; Rare:66 | ||||
| chr3:179451354-179451605 | Common:1; Rare:83 | ||||
| chr3:179604620-179604932 | Common:3; Rare:123 |