chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154503046154503047G-8GENICheterozygous55803585
5154503063154503064T-4GENIChomozygous55803586
5154503115154503116GC20GENICpossibly homozygous55803587
5154503126154503127GC18GENICpossibly homozygous55803588
5154503144154503145GT17GENIChomozygous55803589
5154503146154503147GT17GENICpossibly homozygous55803590
5154516644154516645AG9GENICheterozygous56070851
5154520353154520358GTGTG-----5GENICheterozygous55931010
5154524134154524135A-2GENIChomozygous55803593
5154557488154557489T-5GENICheterozygous56070852
5154557511154557512CT16GENICheterozygous55803596
5154558480154558481T-10GENICheterozygous55931014
5154559540154559542TT--19GENICheterozygous56070853
5154559541154559542T-19GENICheterozygous56070854
5154560256154560257AAT10GENICheterozygous56070855
5154563600154563604GTGT----9GENICheterozygous56070856
5154575556154575557CT16GENIChomozygous56070857
5154577319154577320CA21GENIChomozygous55803598
5154577321154577322CA20GENIChomozygous55803599