Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50192478-50192846 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):9 | ||||
chr17:50194355-50194801 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
chr17:50195050-50195278 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
chr17:50195923-50196190 | Common:2; Rare:72; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr17:50196801-50197073 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr17:50201399-50201486 | Rare:30 | ||||
chr17:50201503-50201897 | Common:2; Rare:102; Clinvar:4; Clinvar (benign):3 | ||||
chr17:50373148-50373239 | Common:2; Rare:43 | ||||
chr17:50397214-50397380 | Common:2; Rare:49 | ||||
chr17:50866351-50866639 | Common:3; Rare:85 | ||||
chr17:51260131-51260581 | Common:3; Rare:165 | ||||
chr17:54968619-54968790 | Common:3; Rare:84 | ||||
chr17:56914022-56914176 | Rare:38 | ||||
chr17:57850008-57850228 | Common:1; Rare:76 | ||||
chr17:57988096-57988265 | Common:1; Rare:46 |