chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213885060213885061AC43GENIChomozygous108532098
1213885125213885126CA44GENIChomozygous108532099
1213885165213885166CT35GENIChomozygous108532102
1213885274213885275TC38GENIChomozygous108532103
1213885572213885573GA28GENIChomozygous108532104
1213886034213886035GA27GENIChomozygous108532105
1213886414213886415AG19GENIChomozygous108532106
1213887070213887071GA19GENIChomozygous108532107
1213887285213887286AG24GENIChomozygous108532108
1213887856213887857AT16GENIChomozygous108532109
1213888171213888172GC37GENIChomozygous108532110
1213888508213888509GT23GENIChomozygous108532111
1213890408213890409AG29GENIChomozygous108532112
1213890487213890488CG20GENIChomozygous108532113
1213893036213893037CT40GENIChomozygous108532114
1213893356213893357AT19GENIChomozygous108532116
1213893368213893369GC22GENIChomozygous108532117
1213893489213893490GA22GENIChomozygous108532118
1213893561213893562CT18GENIChomozygous108532119
1213894158213894159GC24GENICpossibly homozygous108532121
1213894282213894283TC21GENIChomozygous108532122
1213894527213894528AG26GENIChomozygous108532123
1213895761213895762TC28GENIChomozygous108532124
1213896124213896125GA23GENIChomozygous108532125
1213896806213896807CT31GENIChomozygous108532126