| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490719-45490887 | Rare:56 | ||||
| chr17:47323864-47323962 | Rare:37 | ||||
| chr17:47896037-47896269 | Rare:67 | ||||
| chr17:47941374-47941625 | Rare:52; Clinvar:1 | ||||
| chr17:48048069-48048405 | Rare:86 | ||||
| chr17:48048606-48048812 | Common:4; Rare:28 | ||||
| chr17:48944788-48944918 | Common:2; Rare:36 | ||||
| chr17:49210221-49210413 | Common:2; Rare:27 | ||||
| chr17:49210551-49210718 | Rare:26 | ||||
| chr17:49788567-49788724 | Common:1; Rare:49 | ||||
| chr17:50186315-50186695 | Common:2; Rare:100; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:50188533-50189011 | Rare:122; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50189167-50189682 | Rare:117; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192795-50193039 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 |