| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734472-167734728 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr3:167734744-167735237 | Common:3; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735611-167735763 | Rare:37 | ||||
| chr3:168095898-168096052 | Rare:52 | ||||
| chr3:169769501-169769663 | Common:1; Rare:57 | ||||
| chr3:169773322-169773424 | Rare:32 | ||||
| chr3:169812470-169812879 | Common:2; Rare:96 | ||||
| chr3:169966689-169966858 | Rare:71 | ||||
| chr3:170418844-170419297 | Common:1; Rare:101 | ||||
| chr3:170870163-170870335 | Rare:82 | ||||
| chr3:170908578-170908850 | Common:1; Rare:78 | ||||
| chr3:171102049-171102178 | Common:1; Rare:20 | ||||
| chr3:171460054-171460571 | Common:2; Rare:120 | ||||
| chr3:171900462-171900524 | Common:1; Rare:13 | ||||
| chr3:172039469-172039656 | Common:1; Rare:62 |