Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:45060941-45061339 | Common:3; Rare:101 | ||||
chr17:45148142-45148478 | Common:1; Rare:94 | ||||
chr17:45490733-45490887 | Rare:50 | ||||
chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47189235-47189569 | Rare:84 | ||||
chr17:47831516-47831637 | Rare:32 | ||||
chr17:47941363-47941712 | Rare:97; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048568-48048813 | Common:4; Rare:47 | ||||
chr17:48100855-48101097 | Rare:60 | ||||
chr17:48590261-48590428 | Common:1; Rare:37 | ||||
chr17:48944702-48944850 | Rare:52 | ||||
chr17:48997435-48997477 | Rare:8 | ||||
chr17:49677968-49678335 | Rare:92 | ||||
chr17:49788462-49788736 | Common:1; Rare:89 | ||||
chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 |