Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:14300850-14301126 | Common:3; Rare:79 | ||||
chr17:15699521-15699773 | Common:3; Rare:68 | ||||
chr17:15999590-15999981 | Common:3; Rare:177; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:16380757-16381183 | Common:3; Rare:146 | ||||
chr17:17228123-17228374 | Rare:59; Clinvar (benign):1 | ||||
chr17:17495659-17495931 | Common:1; Rare:75 | ||||
chr17:17495981-17496123 | Rare:39 | ||||
chr17:17496388-17496575 | Common:2; Rare:51 | ||||
chr17:17591589-17591922 | Common:2; Rare:94 | ||||
chr17:18087788-18087997 | Rare:57 | ||||
chr17:18183334-18183515 | Rare:43 | ||||
chr17:18183590-18183926 | Common:1; Rare:134 | ||||
chr17:18253308-18253567 | Rare:94 | ||||
chr17:18254596-18254823 | Rare:73 | ||||
chr17:18314887-18315326 | Common:2; Rare:120 |