| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192788-50193048 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194830 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195018-50195667 | Common:1; Rare:183; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50196154-50196370 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:50197947-50198505 | Common:4; Rare:131; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr17:50199524-50199954 | Common:7; Rare:139; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50201391-50201730 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:50201732-50201796 | Rare:19 | ||||
| chr17:50373151-50373249 | Common:3; Rare:44 | ||||
| chr17:50707586-50707963 | Common:4; Rare:110 | ||||
| chr17:50719450-50719713 | Common:1; Rare:109 | ||||
| chr17:50866351-50866560 | Common:2; Rare:65 | ||||
| chr17:51153333-51153649 | Common:1; Rare:80 | ||||
| chr17:51260361-51260607 | Common:3; Rare:116 |