| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44947609-44947936 | Common:1; Rare:85 | ||||
| chr17:45060984-45061347 | Common:2; Rare:100 | ||||
| chr17:45148126-45148615 | Common:1; Rare:163 | ||||
| chr17:45161505-45161780 | Common:1; Rare:71 | ||||
| chr17:45490719-45490887 | Rare:56 | ||||
| chr17:45620232-45620364 | Rare:30 | ||||
| chr17:46193400-46193606 | Common:3; Rare:56 | ||||
| chr17:46922855-46923187 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189235-47189563 | Rare:82 | ||||
| chr17:47530993-47531286 | Rare:73 | ||||
| chr17:47649481-47649980 | Common:2; Rare:179 | ||||
| chr17:47831497-47831654 | Rare:46 | ||||
| chr17:47896147-47896270 | Rare:41 | ||||
| chr17:47941334-47941732 | Rare:106; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48047786-48047883 | Common:1; Rare:18 |