| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47649543-47649965 | Common:1; Rare:155 | ||||
| chr17:47831516-47831656 | Rare:36 | ||||
| chr17:47841201-47841355 | Rare:36 | ||||
| chr17:47896502-47896558 | Rare:13 | ||||
| chr17:47941334-47941802 | Rare:121; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:47970774-47971170 | Common:4; Rare:90 | ||||
| chr17:48048054-48048400 | Rare:93 | ||||
| chr17:48048576-48048827 | Common:4; Rare:47 | ||||
| chr17:48107412-48107817 | Common:6; Rare:100 | ||||
| chr17:48892329-48892507 | Common:9; Rare:62 | ||||
| chr17:48944736-48944928 | Common:2; Rare:72 | ||||
| chr17:48997125-48997671 | Rare:118 | ||||
| chr17:49013732-49013857 | Rare:33 | ||||
| chr17:49210088-49210413 | Common:2; Rare:56 | ||||
| chr17:49210427-49210535 | Common:1; Rare:25 |