chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36785001967850020GA49GENIChomozygous111598635
36785092367850924GA37GENIChomozygous111598636
36785109167851092GA45GENICpossibly homozygous111598637
36785117267851173CT42GENICpossibly homozygous111598638
36785137867851379TC43GENIChomozygous111598639
36785145267851453GA46GENIChomozygous111598640
36785197967851980CT39GENIChomozygous111598641
36785207267852073TC53GENIChomozygous111598642
36785246767852468CT25GENIChomozygous111598643
36785259567852596GA25GENIChomozygous111598644
36785269867852699CT32GENIChomozygous111598645
36785345567853456AG21GENIChomozygous111598646
36785377567853776CT48GENIChomozygous111598647
36785442667854427AG64GENIChomozygous111598648
36785452467854525CT69GENIChomozygous111598649
36785457167854572AT63GENIChomozygous111598650
36785504767855048GA63GENIChomozygous111598651
36785609667856097CA49GENIChomozygous111598652
36785620267856203GC54GENIChomozygous111598653
36785626067856261AT40GENIChomozygous111598654
36785651767856518AG43GENICheterozygous111598655
36785657067856571CT31GENICheterozygous111598656
36785657767856578AG29GENICheterozygous111598657
36785965767859658CT57GENIChomozygous111598658
36786015567860156AG38GENIChomozygous111598659
36786039667860397CT37GENIChomozygous111598660
36786070567860706AG22GENIChomozygous111598661
36786076267860763AG28GENIChomozygous111598662
36786155167861552AG54GENIChomozygous111598663
36786195367861954TG20GENIChomozygous111598664
36786212367862124GA46GENIChomozygous111598665