| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47323890-47324009 | Common:1; Rare:36 | ||||
| chr17:47831516-47831646 | Rare:33 | ||||
| chr17:47941345-47941733 | Rare:104; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048064-48048405 | Rare:90 | ||||
| chr17:48048602-48048813 | Common:4; Rare:30 | ||||
| chr17:48544588-48544652 | Rare:34 | ||||
| chr17:48544716-48544889 | Common:2; Rare:54 | ||||
| chr17:48557104-48557157 | Rare:11 | ||||
| chr17:48590270-48590451 | Common:1; Rare:40 | ||||
| chr17:48908300-48908407 | Common:1; Rare:25 | ||||
| chr17:48944783-48944897 | Common:1; Rare:33 | ||||
| chr17:49210567-49210711 | Rare:21 | ||||
| chr17:50188542-50188771 | Rare:55; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr17:50194588-50194804 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr17:50373168-50373228 | Common:2; Rare:28 |