Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:68512367-68512534 | Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
chr17:69327091-69327340 | Common:2; Rare:81 | ||||
chr17:69414637-69414731 | Rare:17 | ||||
chr17:72120793-72121028 | Rare:61 | ||||
chr17:73232120-73232707 | Common:4; Rare:226 | ||||
chr17:73311963-73312184 | Rare:57 | ||||
chr17:74776272-74776543 | Common:4; Rare:90 | ||||
chr17:75012592-75012719 | Common:1; Rare:37 | ||||
chr17:75087846-75087969 | Common:2; Rare:29 | ||||
chr17:75130854-75131099 | Common:2; Rare:84 | ||||
chr17:75154478-75154802 | Common:1; Rare:100 | ||||
chr17:75205399-75205741 | Rare:102 | ||||
chr17:75261570-75261939 | Common:4; Rare:119; Clinvar (benign):2 | ||||
chr17:75271154-75271356 | Common:2; Rare:37 | ||||
chr17:75289365-75289624 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 |