chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213885060213885061AC25GENIChomozygous108532098
1213885125213885126CA21GENIChomozygous108532099
1213885165213885166CT27GENIChomozygous108532102
1213885274213885275TC27GENIChomozygous108532103
1213885572213885573GA23GENIChomozygous108532104
1213886034213886035GA23GENIChomozygous108532105
1213886414213886415AG30GENIChomozygous108532106
1213887070213887071GA25GENIChomozygous108532107
1213887285213887286AG36GENICpossibly homozygous108532108
1213887856213887857AT19GENIChomozygous108532109
1213888171213888172GC34GENIChomozygous108532110
1213888508213888509GT31GENIChomozygous108532111
1213890408213890409AG23GENIChomozygous108532112
1213890487213890488CG37GENIChomozygous108532113
1213893036213893037CT26GENIChomozygous108532114
1213893356213893357AT26GENIChomozygous108532116
1213893368213893369GC28GENIChomozygous108532117
1213893489213893490GA30GENIChomozygous108532118
1213894158213894159GC22GENICpossibly homozygous108532121
1213894282213894283TC25GENIChomozygous108532122
1213894527213894528AG39GENIChomozygous108532123
1213895761213895762TC29GENIChomozygous108532124
1213896124213896125GA20GENIChomozygous108532125
1213896806213896807CT29GENIChomozygous108532126
1213897524213897525TC18GENIChomozygous108532127
1213897567213897568CT14GENIChomozygous109366979