| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48944736-48944909 | Common:2; Rare:67 | ||||
| chr17:48996970-48997540 | Rare:134 | ||||
| chr17:48998001-48998330 | Common:2; Rare:102 | ||||
| chr17:49230762-49230895 | Common:2; Rare:31 | ||||
| chr17:49677968-49678342 | Rare:93 | ||||
| chr17:49707871-49707991 | Rare:64 | ||||
| chr17:49708152-49708353 | Common:1; Rare:59 | ||||
| chr17:49788462-49788736 | Common:1; Rare:89 | ||||
| chr17:50188740-50189024 | Rare:73; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192797-50193048 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194141-50194450 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194840 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195029-50195700 | Common:1; Rare:186; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50196154-50196368 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 |