| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50192795-50193048 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194783 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50195045-50195331 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):5 | ||||
| chr17:50195425-50195689 | Rare:60; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50196154-50196671 | Common:3; Rare:141; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr17:50197947-50198206 | Common:3; Rare:66; Clinvar (benign):6 | ||||
| chr17:50199554-50199976 | Common:7; Rare:143; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50707976-50708080 | Rare:19 | ||||
| chr17:50719444-50719667 | Common:1; Rare:89 | ||||
| chr17:51120729-51120989 | Rare:105 | ||||
| chr17:51166368-51166955 | Common:4; Rare:160 | ||||
| chr17:51260368-51260598 | Common:3; Rare:109 | ||||
| chr17:54968601-54968792 | Common:3; Rare:90 | ||||
| chr17:55421788-55422195 | Common:3; Rare:131 | ||||
| chr17:56833829-56834116 | Common:2; Rare:78 |