chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106048787760487878AT26GENIChomozygous570162886
106048787860487879AC27GENICpossibly homozygous570162887
106048794960487950TG18GENIChomozygous570162888
106048799260487993AG19GENIChomozygous570162889
106048799760487998CA21GENIChomozygous570162890
106048802560488026AT23GENIChomozygous570162891
106048803560488036GA24GENIChomozygous570162892
106048806360488064TA27GENIChomozygous570162893
106048822360488224CT17GENIChomozygous570162894
106048832760488328AG18GENIChomozygous570162895
106048834960488350CT16GENIChomozygous570162896
106048835660488357TC15GENIChomozygous570162897
106048838660488387AT11GENIChomozygous570162898
106048845060488451GA24GENIChomozygous571910241
106048846260488463TC27GENIChomozygous571910242
106048861060488611AG18GENIChomozygous571910243