| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49230696-49230932 | Common:3; Rare:66 | ||||
| chr17:49362443-49362792 | Common:1; Rare:92 | ||||
| chr17:49414845-49415120 | Common:1; Rare:66 | ||||
| chr17:49708132-49708344 | Common:1; Rare:68 | ||||
| chr17:49719893-49719919 | Rare:6 | ||||
| chr17:49788576-49788778 | Common:1; Rare:68 | ||||
| chr17:50095034-50095444 | Common:2; Rare:126 | ||||
| chr17:50188901-50189172 | Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50189248-50189479 | Rare:53; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:50373151-50373253 | Common:3; Rare:47 | ||||
| chr17:50426014-50426252 | Common:2; Rare:63 | ||||
| chr17:50719469-50719786 | Rare:111 | ||||
| chr17:50866340-50866805 | Common:3; Rare:124 | ||||
| chr17:51120709-51120983 | Rare:108 | ||||
| chr17:51166328-51166508 | Common:2; Rare:41 |