| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:65465914-65466036 | Common:2; Rare:28 | ||||
| chr3:65466494-65466707 | Rare:35 | ||||
| chr3:66380716-66381177 | Common:5; Rare:163 | ||||
| chr3:66382431-66382437 | Rare:1 | ||||
| chr3:66480482-66480780 | Common:2; Rare:52 | ||||
| chr3:69060306-69060542 | Common:1; Rare:45 | ||||
| chr3:70968128-70968327 | Common:1; Rare:45 | ||||
| chr3:71040736-71040872 | Common:1; Rare:24 | ||||
| chr3:71057786-71058060 | Common:3; Rare:50 | ||||
| chr3:71101253-71101290 | Common:1; Rare:7 | ||||
| chr3:71112560-71112870 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:71244302-71244486 | Rare:37 | ||||
| chr3:75435011-75435371 | Common:5; Rare:126 | ||||
| chr3:75670144-75670307 | |||||
| chr3:75672088-75672330 | Common:16; Rare:6 |