Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40820590-40820728 | Common:1; Rare:46 | ||||
chr17:41502547-41502719 | Rare:56; Clinvar (benign):2 | ||||
chr17:41503387-41503720 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):3 | ||||
chr17:41526267-41526471 | Common:4; Rare:36 | ||||
chr17:43002750-43002847 | Common:1; Rare:34 | ||||
chr17:43315647-43315916 | Common:6; Rare:114 | ||||
chr17:43388303-43388385 | Rare:17 | ||||
chr17:44797748-44797917 | Rare:27 | ||||
chr17:50189832-50189924 | Common:2; Rare:19; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:50190174-50190381 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
chr17:50193111-50193349 | Rare:36 | ||||
chr17:50197157-50197272 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
chr17:50197592-50197821 | Common:1; Rare:54; Clinvar:3 | ||||
chr17:50197828-50198011 | Common:3; Rare:55; Clinvar (benign):6 | ||||
chr17:58324403-58324542 | Rare:42 |