| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:168251395-168251641 | Common:3; Rare:37 | ||||
| chr3:168715038-168715121 | Rare:15 | ||||
| chr3:169764282-169764718 | Common:2; Rare:109; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:169764937-169765338 | Common:1; Rare:130; Clinvar:7; Clinvar (pathogenic):6 | ||||
| chr3:169771875-169771909 | Rare:9 | ||||
| chr3:169772000-169772271 | Common:3; Rare:123 | ||||
| chr3:169813832-169814140 | Common:3; Rare:59 | ||||
| chr3:169865451-169865692 | Common:2; Rare:52 | ||||
| chr3:169932110-169932524 | Common:2; Rare:93 | ||||
| chr3:169940457-169940712 | Common:3; Rare:39 | ||||
| chr3:169945414-169945555 | Rare:29 | ||||
| chr3:169954266-169954404 | Rare:19 | ||||
| chr3:169954958-169954999 | Rare:6 | ||||
| chr3:169965513-169965781 | Common:3; Rare:58 | ||||
| chr3:169965787-169965836 | Rare:10 |