| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48048058-48048405 | Rare:93 | ||||
| chr17:48048599-48048833 | Common:4; Rare:38 | ||||
| chr17:48722450-48722610 | Rare:25 | ||||
| chr17:48722966-48723233 | Rare:60 | ||||
| chr17:48723641-48723684 | Rare:9 | ||||
| chr17:48944773-48944924 | Common:2; Rare:50 | ||||
| chr17:49210572-49210727 | Rare:24 | ||||
| chr17:49414845-49415134 | Common:2; Rare:70 | ||||
| chr17:49707865-49707971 | Rare:58 | ||||
| chr17:49708148-49708390 | Common:1; Rare:76 | ||||
| chr17:49788557-49788759 | Common:1; Rare:69 | ||||
| chr17:50199765-50200092 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50373168-50373256 | Common:3; Rare:37 | ||||
| chr17:50426072-50426252 | Common:1; Rare:44 | ||||
| chr17:50719456-50719661 | Rare:81 |