| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47821185-47821228 | Common:1; Rare:9 | ||||
| chr17:47821708-47821899 | Common:2; Rare:45 | ||||
| chr17:47831501-47831689 | Rare:55 | ||||
| chr17:47841199-47841390 | Rare:42 | ||||
| chr17:47896084-47896270 | Rare:55 | ||||
| chr17:47941341-47941750 | Rare:110; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47957765-47958029 | Common:1; Rare:48 | ||||
| chr17:48048058-48048405 | Rare:93 | ||||
| chr17:48048602-48048864 | Common:4; Rare:42 | ||||
| chr17:48101254-48101637 | Common:3; Rare:105 | ||||
| chr17:48107427-48107825 | Common:5; Rare:97 | ||||
| chr17:48544219-48544335 | Common:1; Rare:15 | ||||
| chr17:48544558-48544644 | Rare:42 | ||||
| chr17:48544711-48544728 | Common:1; Rare:5 | ||||
| chr17:48590237-48590428 | Common:1; Rare:42 |