| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167735577-167735770 | Rare:51; Clinvar:1 | ||||
| chr3:168095107-168095204 | Rare:27 | ||||
| chr3:168095584-168095981 | Common:4; Rare:111 | ||||
| chr3:169769542-169769834 | Common:2; Rare:96 | ||||
| chr3:169772748-169772860 | Rare:25 | ||||
| chr3:169773270-169773465 | Common:1; Rare:71 | ||||
| chr3:169812875-169813106 | Common:2; Rare:46 | ||||
| chr3:169966706-169966870 | Rare:67 | ||||
| chr3:169982751-169983252 | Common:1; Rare:105 | ||||
| chr3:170037961-170038219 | Common:5; Rare:66 | ||||
| chr3:170358200-170358611 | Common:4; Rare:138 | ||||
| chr3:170870150-170870313 | Rare:87 | ||||
| chr3:170870432-170870542 | Rare:18 | ||||
| chr3:170908556-170908862 | Common:1; Rare:91 | ||||
| chr3:171460258-171460645 | Rare:94 |