| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50195420-50195672 | Rare:59; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50196153-50196231 | Rare:29; Clinvar (benign):2 | ||||
| chr17:50196299-50196677 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50198054-50198511 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50199145-50199329 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50199548-50199962 | Common:7; Rare:134; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50200103-50200355 | Common:1; Rare:63 | ||||
| chr17:50200505-50200813 | Rare:69 | ||||
| chr17:50201224-50201863 | Common:2; Rare:164; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:50373160-50373253 | Common:3; Rare:41 | ||||
| chr17:50426116-50426257 | Rare:34 | ||||
| chr17:50719459-50719818 | Rare:120 | ||||
| chr17:50866316-50866557 | Common:3; Rare:81 | ||||
| chr17:51166289-51166547 | Common:2; Rare:60 | ||||
| chr17:51260367-51260575 | Common:3; Rare:94 |