| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47586165-47586382 | Common:3; Rare:37 | ||||
| chr17:47649489-47649880 | Common:2; Rare:119 | ||||
| chr17:47831501-47831674 | Rare:49 | ||||
| chr17:47941354-47941712 | Rare:97; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48037672-48037865 | Common:5; Rare:45 | ||||
| chr17:48048048-48048453 | Rare:115 | ||||
| chr17:48048557-48048821 | Common:4; Rare:52 | ||||
| chr17:48107687-48107828 | Common:1; Rare:38 | ||||
| chr17:48944758-48944958 | Common:2; Rare:69 | ||||
| chr17:49414830-49415119 | Common:1; Rare:68 | ||||
| chr17:49708144-49708362 | Common:1; Rare:63 | ||||
| chr17:49788560-49788727 | Common:1; Rare:53 | ||||
| chr17:50186315-50186958 | Common:2; Rare:188; Clinvar:17; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr17:50188745-50188965 | Rare:63; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50191776-50192026 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 |