| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50055697-50055809 | Common:2; Rare:22 | ||||
| chr17:50186315-50186923 | Common:2; Rare:169; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188740-50189011 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50189167-50189682 | Rare:117; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:50192474-50192651 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:50192797-50193029 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194829 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195231-50195668 | Rare:117; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50196179-50196324 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:50197948-50198498 | Common:4; Rare:131; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr17:50199554-50199948 | Common:7; Rare:133; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50373168-50373259 | Common:3; Rare:38 | ||||
| chr17:50719410-50719724 | Common:1; Rare:130 | ||||
| chr17:50866348-50866543 | Common:2; Rare:64 | ||||
| chr17:51153292-51153649 | Common:1; Rare:92 |