| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49707871-49708028 | Rare:74 | ||||
| chr17:49708129-49708369 | Common:1; Rare:74 | ||||
| chr17:49788576-49788774 | Common:1; Rare:64 | ||||
| chr17:50055697-50056001 | Common:4; Rare:57 | ||||
| chr17:50095037-50095444 | Common:2; Rare:126 | ||||
| chr17:50165697-50166060 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:50186315-50186928 | Common:2; Rare:173; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188740-50189276 | Rare:136; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50191786-50192027 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192779-50193048 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr17:50194129-50194449 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194829 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195018-50195684 | Common:1; Rare:183; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50196154-50196360 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):2 |