chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103671632136716322GT10GENIChomozygous116561632
103671663236716633TC14GENIChomozygous116561634
103671714836717149CA12GENIChomozygous116561636
103671799636717997AG9GENIChomozygous116561638
103671900836719009TC11GENIChomozygous116759703
103671910136719102AG11GENIChomozygous116561640
103671989236719893GA14GENIChomozygous116561642
103672187836721879AG19GENIChomozygous116561646
103672193236721933AG13GENIChomozygous116561648
103672310436723105TC17GENIChomozygous116561650
103672325336723254TC12GENIChomozygous116561652
103672515336725154AG20GENIChomozygous116561654
103672679336726794AG20GENIChomozygous116759705
103672778336727784GC22GENIChomozygous116561656
103671981436719815A15GENIChomozygous128808083
103672361836723619T8GENIChomozygous128808084
103672765236727653T22GENIChomozygous128808085
103672840536728405A15GENIChomozygous128808086
103672888436728885TA16GENIChomozygous116561658
103672965136729652AG14GENIChomozygous116759707
103673006936730070AT15GENIChomozygous116561660
103673007036730071GC15GENIChomozygous116561662
103673052836730532GTAG13GENIChomozygous128808087
103673278236732783CG18GENIChomozygous116561668
103673343236733433CT19GENIChomozygous116561670
103673344036733441TG17GENIChomozygous116561672
103673345936733459A17GENIChomozygous128808088