chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109113309491133095CT6GENIChomozygous117068583
109113571691135717AG37GENIChomozygous116905431
109113439291134393AG26GENIChomozygous116905425
109113455791134558CT22GENIChomozygous116905427
109113490091134901TA24GENIChomozygous116905429
109113615691136157AG14GENIChomozygous116905433
109114030391140304AT23GENIChomozygous116905435
109114030491140305GA23GENIChomozygous116905437
109114123991141240TC21GENIChomozygous116905439
109114655491146555TC18GENIChomozygous116905441
109114736291147363AG11GENIChomozygous116905443
109114947091149471AG15GENIChomozygous116905445
109114955991149560AT23GENIChomozygous116905447
109114957991149580TC23GENIChomozygous116905449
109115073591150736TC30GENIChomozygous116905451
109115204091152041CT26GENIChomozygous116905453
109115769291157693GA23GENIChomozygous116905455
109115806091158061GT20GENIChomozygous117068585
109115967291159673TC16GENIChomozygous116905457
109115980191159802GA25GENIChomozygous116905459
109116031191160312AG17GENIChomozygous116905461
109115554091155541T19GENIChomozygous131708983
109114058691140586TGAG19GENIChomozygous131708980
109114752391147524G14GENIChomozygous131708981
109115358691153586T20GENIChomozygous131708982
109115731791157318C12GENIChomozygous131708984
109115611291156113GC14GENIChomozygous118007841