chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213885060213885061AC48GENIChomozygous108532098
1213885125213885126CA47GENIChomozygous108532099
1213885145213885153CGCACACA45GENIChomozygous127481039
1213885165213885166CT47GENIChomozygous108532102
1213885274213885275TC48GENIChomozygous108532103
1213885572213885573GA46GENIChomozygous108532104
1213886034213886035GA58GENIChomozygous108532105
1213886414213886415AG40GENIChomozygous108532106
1213887070213887071GA37GENIChomozygous108532107
1213887285213887286AG52GENIChomozygous108532108
1213887856213887857AT53GENICpossibly homozygous108532109
1213888171213888172GC49GENIChomozygous108532110
1213888508213888509GT48GENIChomozygous108532111
1213890408213890409AG41GENIChomozygous108532112
1213890487213890488CG41GENIChomozygous108532113
1213892092213892094TG37GENIChomozygous127481040
1213892924213892925T56GENIChomozygous127481041
1213893036213893037CT50GENIChomozygous108532114
1213893356213893357AT39GENIChomozygous108532116
1213893368213893369GC40GENIChomozygous108532117
1213893489213893490GA42GENIChomozygous108532118
1213893561213893562CT29GENIChomozygous108532119
1213893641213893642AG25GENIChomozygous108532120
1213894158213894159GC45GENIChomozygous108532121
1213894229213894232CTT39GENIChomozygous127481042
1213894282213894283TC48GENIChomozygous108532122
1213894527213894528AG42GENIChomozygous108532123
1213895174213895174G50GENIChomozygous127481043
1213895413213895419CAGAGG61GENIChomozygous127481044
1213895761213895762TC63GENIChomozygous108532124
1213896124213896125GA64GENIChomozygous108532125
1213896806213896807CT47GENIChomozygous108532126
1213897523213897523C30GENIChomozygous127481045
1213897637213897637TGAC50GENIChomozygous127481046
1213897567213897568CT25GENIChomozygous109366979