chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103671632136716322GT18GENIChomozygous116561632
103671663236716633TC27GENIChomozygous116561634
103671714836717149CA27GENICpossibly homozygous116561636
103671799636717997AG17GENIChomozygous116561638
103671910136719102AG31GENIChomozygous116561640
103671989236719893GA25GENIChomozygous116561642
103672125036721251AG23GENIChomozygous116561644
103672187836721879AG31GENIChomozygous116561646
103672193236721933AG31GENIChomozygous116561648
103672310436723105TC19GENIChomozygous116561650
103672325336723254TC23GENIChomozygous116561652
103672515336725154AG33GENIChomozygous116561654
103672778336727784GC22GENIChomozygous116561656
103672840536728405A25GENIChomozygous128808086
103671981436719815A11GENIChomozygous128808083
103672361836723619T16GENIChomozygous128808084
103672765236727653T19GENIChomozygous128808085
103672888436728885TA21GENIChomozygous116561658
103673006936730070AT17GENIChomozygous116561660
103673007036730071GC17GENIChomozygous116561662
103673038136730382TC18GENIChomozygous116561664
103673052836730532GTAG16GENIChomozygous128808087
103673163636731637GA22GENIChomozygous116561666
103673278236732783CG24GENIChomozygous116561668
103673343236733433CT18GENIChomozygous116561670
103673344036733441TG16GENIChomozygous116561672
103673345936733459A20GENIChomozygous128808088