| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21287651-21288223 | Common:1; Rare:216 | ||||
| chr17:27293931-27294182 | Common:4; Rare:197 | ||||
| chr17:27456279-27456506 | Common:1; Rare:71 | ||||
| chr17:28318882-28319357 | Common:6; Rare:300 | ||||
| chr17:28335370-28335839 | Common:2; Rare:216 | ||||
| chr17:28357436-28357739 | Common:10; Rare:279; Clinvar (pathogenic):2 | ||||
| chr17:28370225-28370422 | Rare:51 | ||||
| chr17:28370404-28370696 | Common:3; Rare:62 | ||||
| chr17:28406115-28406268 | Rare:29; Clinvar:1 | ||||
| chr17:28552572-28552791 | Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571474-28571681 | Rare:87 | ||||
| chr17:28576826-28577062 | Common:2; Rare:58 | ||||
| chr17:28598898-28599174 | Common:5; Rare:159 | ||||
| chr17:28644660-28645040 | Common:1; Rare:125 | ||||
| chr17:28645043-28645366 | Common:2; Rare:249 |