Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41688661-41688899 | Common:1; Rare:79 | ||||
chr17:41689296-41689937 | Common:4; Rare:194 | ||||
chr17:41812848-41813029 | Rare:50; Clinvar:2 | ||||
chr17:41966614-41966837 | Common:1; Rare:80 | ||||
chr17:42017367-42017487 | Rare:53 | ||||
chr17:42388576-42388887 | Common:1; Rare:78 | ||||
chr17:42423064-42423283 | Rare:69; Clinvar:2 | ||||
chr17:42458748-42458938 | Common:3; Rare:70 | ||||
chr17:42566926-42567149 | Common:3; Rare:80 | ||||
chr17:42577658-42577838 | Rare:85 | ||||
chr17:42609326-42609743 | Common:8; Rare:178; Clinvar (benign):2 | ||||
chr17:42676954-42677292 | Common:1; Rare:90 | ||||
chr17:42682429-42682557 | Rare:29 | ||||
chr17:42761075-42761254 | Rare:50 | ||||
chr17:42761316-42761346 | Rare:8 |