chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106367635563676356TG10GENIChomozygous116616348
106367770663677707AT3GENIChomozygous116940601
106368205763682058TC8GENIChomozygous116616358
106368305363683054GA17GENIChomozygous116940603
106368418063684181CT22GENIChomozygous116940605
106368804863688049CT20GENIChomozygous116616362
106369319963693200CT21GENIChomozygous116940607
106369383263693833GT15GENIChomozygous116616370
106369417163694172AT13GENIChomozygous116940609
106369639663696397CT11GENIChomozygous116940611
106369913163699132AG23GENIChomozygous116940613
106370184263701843TG41GENIChomozygous116616380
106370329863703299TC14GENIChomozygous116616392
106370367863703679AG18GENIChomozygous116616396
106370863063708631CT27GENIChomozygous116940615
106370986963709870AG8GENIChomozygous116616418
106371094263710943AT15GENIChomozygous116616424
106371408163714082AT9GENIChomozygous116978547
106371873063718731AT19GENIChomozygous116940617