| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45051571-45051688 | Rare:42 | ||||
| chr17:45060993-45061345 | Common:2; Rare:96 | ||||
| chr17:45132340-45132639 | Common:2; Rare:89 | ||||
| chr17:45148159-45148482 | Common:1; Rare:95 | ||||
| chr17:45148596-45148608 | Rare:4 | ||||
| chr17:45490719-45490867 | Rare:51 | ||||
| chr17:46192896-46193019 | Common:1; Rare:33 | ||||
| chr17:46193509-46193595 | Common:1; Rare:27 | ||||
| chr17:46923048-46923187 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47323890-47324013 | Common:1; Rare:40 | ||||
| chr17:47831516-47831656 | Rare:36 | ||||
| chr17:47941352-47941724 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970736-47971064 | Common:4; Rare:73 | ||||
| chr17:48048061-48048400 | Rare:90 | ||||
| chr17:48048643-48048813 | Common:3; Rare:23 |