chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168910387168910388AG27GENIChomozygous62538590
1168910650168910651TG21GENIChomozygous62538591
1168910783168910784AACT33GENIChomozygous62538592
1168910809168910810CG32GENIChomozygous62538593
1168910966168910967TC20GENIChomozygous60937182
1168910987168910988GA19GENIChomozygous62538594
1168911127168911128GA23GENIChomozygous62538595
1168911546168911547TC24GENIChomozygous62538596
1168911637168911638TG25GENICpossibly homozygous62538597
1168911927168911928GGGCAGACCCTAAACCATCT19GENIChomozygous62538598
1168911948168911949GA19GENIChomozygous62538599
1168912075168912076CG20GENIChomozygous60937184
1168912240168912241AG18GENIChomozygous62538600
1168912272168912273CT14GENIChomozygous62538601
1168912651168912652TC18GENIChomozygous62538602
1168913249168913250GA23GENIChomozygous62538603
1168913472168913480GCACACAC--------5GENICheterozygous62247701
1168913691168913692GGTA29GENIChomozygous62538604
1168913898168913899GA23GENIChomozygous62538605
1168914296168914297GA26GENIChomozygous62538606
1168914305168914306GA26GENIChomozygous62538607
1168914372168914373T-20GENICpossibly homozygous62544835
1168914385168914386TC20GENICpossibly homozygous62538608
1168914634168914635AT21GENIChomozygous62538609
1168914871168914872GA24GENIChomozygous62538610
1168914984168914985TG30GENIChomozygous62538611
1168915121168915122CT21GENIChomozygous62538612
1168916790168916791CT19GENIChomozygous62538613
1168916880168916881CCGTTT14GENICheterozygous62091355
1168917084168917085AG20GENIChomozygous60937195
1168917464168917465GA32GENIChomozygous62538614
1168918752168918753T-21GENIChomozygous60937198
1168913471168913481CGCACACACA----------5GENICheterozygous62172499