chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18620806086208061AG49GENIChomozygous61456419
18620943986209440TC57GENIChomozygous61456427
18621148486211492TACTTTAA--------25GENIChomozygous61456429
18621156286211563GA50GENICpossibly homozygous62013638
18621214986212150GA58GENIChomozygous62013639
18621260286212603TTA45GENIChomozygous61456433
18621292786212929CA--22GENIChomozygous61297442
18621308986213090AG40GENICheterozygous62013640
18621309386213094AG39GENICheterozygous62013641
18621356186213562AAT29GENIChomozygous60748913
18621412786214128CT40GENIChomozygous62013642
18621453586214536AG50GENIChomozygous61456439
18621456586214566GA44GENIChomozygous62013643
18621524286215243TC55GENICheterozygous62013644
18621525086215251TC55GENICheterozygous62013645
18621548486215494ACACACACAC----------9GENIChomozygous62013646
18621743386217434AG5GENIChomozygous61669876
18621750686217507CCG4GENIChomozygous60748917
18621751486217515CG4GENIChomozygous60748919
18621752286217523T-5GENIChomozygous60748921
18621753286217533T-7GENIChomozygous60748923
18621754486217545G-17GENIChomozygous60748925
18621756186217562CCA18GENIChomozygous60748927
18621786186217862AAAC4GENICheterozygous61456448
18621825386218254TTC63GENIChomozygous62013647
18621874186218742AG21GENIChomozygous61456449