chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22757411927574120GA18GENIChomozygous111094659
22758111427581115GA16GENIChomozygous111094661
22758308427583085CT19GENIChomozygous111094663
22761801727618018CT22GENIChomozygous111094675
22765411527654116AG24GENIChomozygous109660438
22766303927663040GA36GENIChomozygous109660518
22766729427667295GC26GENIChomozygous109660530
22767448327674484CG12GENIChomozygous109660548
22767695027676951TC30GENIChomozygous111094708
22768252827682529AG31GENIChomozygous109660562
22768659927686600AG28GENIChomozygous109660572
22769113927691140GA7GENIChomozygous111094712
22769336327693364TC17GENIChomozygous109660584
22769542927695430GA30GENIChomozygous111094715
22770725627707257GA20GENIChomozygous111094726
22771475127714752GT13GENICheterozygous120286519
22771543227715433GT11GENIChomozygous111094735
22771543627715437GT11GENIChomozygous111094737
22771808527718086AT31GENIChomozygous109660626
22771809927718100CG30GENIChomozygous120122660
22771810027718101TC30GENIChomozygous120122662
22771930927719310TC30GENIChomozygous109660632
22771954727719548AT20GENIChomozygous109660633
22772245427722455TG27GENIChomozygous109660655
22772922027729221AG31GENIChomozygous111094739
22773070527730706GA28GENIChomozygous109660679
22773091927730920GT35GENIChomozygous109660687
22773092127730922GA33GENIChomozygous109660689
22773125227731253TG37GENIChomozygous111094741
22773149127731492AG22GENIChomozygous111094743
22773151927731520TC29GENIChomozygous111094745
22773194727731948TG21GENIChomozygous111094747
22773240627732407GC23GENICpossibly homozygous111094750