Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:47649613-47649999 | Common:1; Rare:144 | ||||
chr17:47831462-47831670 | Rare:67 | ||||
chr17:48048020-48048372 | Common:1; Rare:95 | ||||
chr17:48048593-48048829 | Common:4; Rare:37 | ||||
chr17:48544415-48544656 | Common:1; Rare:90 | ||||
chr17:48590231-48590435 | Common:1; Rare:45 | ||||
chr17:48944741-48944918 | Common:2; Rare:65 | ||||
chr17:49788567-49788702 | Rare:37 | ||||
chr17:50056011-50056133 | Common:1; Rare:36 | ||||
chr17:50189220-50189438 | Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
chr17:50196157-50196355 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
chr17:50197047-50197242 | Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
chr17:50373151-50373229 | Common:2; Rare:39 | ||||
chr17:54968631-54968770 | Common:3; Rare:68 | ||||
chr17:57850015-57850274 | Common:1; Rare:78 |