Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50194414-50194829 | Common:3; Rare:122; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
chr17:50195046-50195667 | Common:1; Rare:174; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr17:50201409-50201804 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):4 | ||||
chr17:50373166-50373253 | Common:3; Rare:36 | ||||
chr17:50719467-50719661 | Rare:76 | ||||
chr17:51260061-51260142 | Rare:19 | ||||
chr17:51260386-51260587 | Common:3; Rare:99 | ||||
chr17:54968599-54968798 | Common:3; Rare:93 | ||||
chr17:56914038-56914181 | Rare:32 | ||||
chr17:57084986-57085328 | Rare:116 | ||||
chr17:57849995-57850285 | Common:1; Rare:96 | ||||
chr17:58219216-58219372 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):4 | ||||
chr17:58692361-58692643 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):16 | ||||
chr17:59106701-59106999 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155156-59155694 | Common:2; Rare:134 |