chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG31GENIChomozygous114092623
5172491197172491198CT21GENICpossibly homozygous119189108
5172491314172491315CT29GENIChomozygous119189109
5172492247172492248TC17GENICpossibly homozygous119189111
5172492253172492254CT19GENICpossibly homozygous119189112
5172492753172492754AT32GENICpossibly homozygous119207203
5172493271172493272CT34GENICpossibly homozygous119189113
5172493291172493292GA28GENIChomozygous119189114
5172493570172493571GC23GENICpossibly homozygous119189115
5172494808172494809TC37GENIChomozygous119189116
5172494883172494884CT47GENIChomozygous119189117
5172496684172496685CT26GENICpossibly homozygous119189118
5172496946172496947TC34GENICpossibly homozygous119189119
5172497364172497365CT16GENIChomozygous114092625
5172499650172499651GA27GENICpossibly homozygous119189120
5172499683172499684AG27GENICpossibly homozygous119189121
5172499955172499956CT28GENICpossibly homozygous119189122
5172505834172505835GA22GENICpossibly homozygous119189123
5172514486172514487GA29GENIChomozygous119189124
5172517554172517555CT43GENIChomozygous119189125
5172522126172522127AG25GENIChomozygous119189126
5172525073172525074TC28GENIChomozygous114092669