| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44911517-44911583 | Common:2; Rare:15; Clinvar:1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45132367-45132631 | Common:1; Rare:81 | ||||
| chr17:45148159-45148478 | Common:1; Rare:93 | ||||
| chr17:46922864-46923187 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189111-47189396 | Common:1; Rare:78 | ||||
| chr17:47895911-47896274 | Rare:119 | ||||
| chr17:47941356-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048653-48048862 | Common:3; Rare:33 | ||||
| chr17:48944773-48944894 | Common:1; Rare:40 | ||||
| chr17:49210228-49210441 | Common:2; Rare:31 | ||||
| chr17:49210548-49210721 | Rare:27 | ||||
| chr17:49788576-49788778 | Common:1; Rare:68 | ||||
| chr17:50165961-50166060 | Common:1; Rare:37; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:50373143-50373235 | Common:2; Rare:45 |