chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174983398249833983CG55GENIChomozygous111059918
174984035849840359CT17GENIChomozygous111059919
174985404649854047GA17GENIChomozygous111059921
174985559949855600TA31GENIChomozygous111059922
174985566649855667AG54GENIChomozygous111059923
174985625449856255TG17GENIChomozygous111059924
174987062549870626GA4GENIChomozygous111059925
174987124749871248GA10GENIChomozygous111059926
174987309949873100CA25GENIChomozygous111059927
174988001749880018GT9GENIChomozygous111059928
174988001949880020GT9GENIChomozygous111059929
174988003049880031TC8GENIChomozygous111059930
174988159549881596CA17GENIChomozygous111059931
174988456349884564TG22GENIChomozygous111059932
174988838849888389GC8GENIChomozygous111059933
174989089849890899CT18GENIChomozygous111059934
174989146149891462GA2GENIChomozygous111246389
174989146349891464AT2GENIChomozygous111246391
174989146449891465CT2GENIChomozygous111246393
174989232549892326AG41GENIChomozygous111059936
174989383949893840CT17GENIChomozygous111059937
174989143949891440GT2GENIChomozygous111204254
174989145849891459GA2GENIChomozygous111204255
174989885749898858GA16GENIChomozygous111500638
174989891349898914CT19GENIChomozygous111059938
174989913949899140GT14GENIChomozygous111059940
174989916449899165AG13GENIChomozygous111246397
174991250449912505TC20GENICpossibly homozygous111059943
174991267249912673AG32GENIChomozygous111059944
174991267349912674TC33GENIChomozygous111059945
174991460249914603AT7GENIChomozygous111059946
174991509949915100AG27GENIChomozygous111059947
174992032349920324GC44GENIChomozygous111059948
174992115849921159GA42GENIChomozygous111059949