chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171013597510135976CG33GENIChomozygous110953758
171013598310135984GA35GENIChomozygous110953760
171013679910136800GA8GENIChomozygous111230468
171013695810136959AG10GENIChomozygous110953762
171013915310139154GA22GENIChomozygous111230470
171014168410141685GC30GENIChomozygous110953772
171014664710146648GA31GENIChomozygous111230472
171014877810148779TC22GENIChomozygous111230474
171014903310149034TC24GENIChomozygous110953786
171014932010149321GT23GENIChomozygous110953788
171014938910149390CG23GENIChomozygous110953790
171014939710149398CT22GENIChomozygous110953792
171014941910149420GT22GENIChomozygous110953794
171014949910149500AG19GENIChomozygous110953796
171014955510149556CT19GENIChomozygous110953798
171014961010149611GC17GENIChomozygous110953800
171015035910150360GA25GENIChomozygous110953802
171015038910150390AG27GENIChomozygous110953804
171015073910150740GA16GENIChomozygous110953806
171015080610150807CT21GENIChomozygous110953808
171015088610150887TC17GENIChomozygous110953810
171015106010151061TG29GENIChomozygous110953813
171015121610151217TC21GENIChomozygous110953815
171015129110151292AG20GENIChomozygous110953817
171015133810151339GT23GENIChomozygous110953819
171015141510151416AG30GENIChomozygous110953821
171015149910151500GT22GENIChomozygous110953823
171015158910151590AG32GENIChomozygous110953825
171015169810151699AG27GENIChomozygous110953827
171015180110151802GA26GENIChomozygous110953829
171015221110152212GT20GENIChomozygous110953831
171015232410152325TC24GENIChomozygous110953833