Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7219736-7219981 | Common:3; Rare:98; Clinvar:6; Clinvar (benign):2 | ||||
chr17:7223675-7223869 | Rare:56; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
chr17:7251690-7251741 | Common:1; Rare:13 | ||||
chr17:7251945-7252321 | Common:2; Rare:150 | ||||
chr17:7479517-7479710 | Common:1; Rare:32 | ||||
chr17:7484215-7484370 | Common:1; Rare:61 | ||||
chr17:7583510-7583886 | Common:1; Rare:150; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:7584074-7584133 | Rare:14 | ||||
chr17:7687476-7687596 | Rare:27 | ||||
chr17:7857909-7858095 | Rare:65 | ||||
chr17:7931902-7932308 | Common:5; Rare:111 | ||||
chr17:8189342-8189472 | Common:1; Rare:51 | ||||
chr17:8295346-8295506 | Common:1; Rare:41 | ||||
chr17:10697488-10697653 | Common:3; Rare:72; Clinvar:5; Clinvar (benign):2 | ||||
chr17:10729973-10730128 | Common:3; Rare:34 |