| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49788557-49788750 | Common:1; Rare:64 | ||||
| chr17:50186315-50186923 | Common:2; Rare:169; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188517-50189017 | Rare:126; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50189167-50189539 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:50192474-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192797-50193039 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50193949-50194376 | Common:2; Rare:115; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:50194571-50194829 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195231-50195667 | Rare:117; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50196165-50196324 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:50197946-50198206 | Common:3; Rare:66; Clinvar (benign):6 | ||||
| chr17:50373151-50373257 | Common:3; Rare:48 | ||||
| chr17:50426075-50426252 | Common:1; Rare:42 | ||||
| chr17:50719444-50719647 | Common:1; Rare:80 | ||||
| chr17:50866351-50866560 | Common:2; Rare:65 |