chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X110903269110903270GA11GENIChomozygous801336874
X110903511110903512GC9GENIChomozygous801336875
X110904646110904647TC29GENICheterozygous801336876
X110905948110905949GA57GENICheterozygous801336877
X110905974110905975CA45GENICheterozygous801336878
X110906891110906892CT8GENIChomozygous801336879
X110906892110906893CT8GENIChomozygous801336880
X110911116110911117CA18GENIChomozygous801336881
X110915485110915486CA32GENICheterozygous801336882
X110915561110915562TG90GENICheterozygous801336883
X110916411110916412GA24GENICheterozygous801336884
X110916417110916418GC20GENICheterozygous801336885
X110916420110916421AG20GENICheterozygous801336886
X110918615110918616CT35GENICheterozygous801336887
X110918638110918639CT35GENICheterozygous801336888
X110918709110918710TC31GENICheterozygous801336889
X110918731110918732GT21GENICheterozygous801336890
X110918738110918739CT21GENICheterozygous801336891
X110918746110918747CT24GENICheterozygous801336892
X110918748110918749GA23GENICheterozygous801336893
X110931759110931760TC2GENIChomozygous801336894
X110932836110932837GA2GENIChomozygous801336895
X110932839110932840CA2GENIChomozygous801336896
X110933841110933842CT6GENIChomozygous801336897
X110940136110940137GT4GENIChomozygous801336898
X110940211110940212GA10GENIChomozygous801336899
X110947015110947016TG5GENIChomozygous801336900
X110952545110952546GA5GENIChomozygous801336901
X110975209110975210GA49GENICheterozygous801336902