chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213885060213885061AC24GENIChomozygous108532098
1213885125213885126CA24GENIChomozygous108532099
1213885145213885153CGCACACA24GENIChomozygous127481039
1213885165213885166CT25GENIChomozygous108532102
1213885274213885275TC21GENIChomozygous108532103
1213885572213885573GA15GENIChomozygous108532104
1213886034213886035GA23GENIChomozygous108532105
1213886414213886415AG18GENIChomozygous108532106
1213887070213887071GA21GENIChomozygous108532107
1213887285213887286AG21GENIChomozygous108532108
1213887856213887857AT20GENIChomozygous108532109
1213888171213888172GC10GENICpossibly homozygous108532110
1213888508213888509GT16GENIChomozygous108532111
1213890408213890409AG17GENIChomozygous108532112
1213890487213890488CG14GENIChomozygous108532113
1213892092213892094TG17GENIChomozygous127481040
1213892924213892925T20GENIChomozygous127481041
1213893036213893037CT17GENIChomozygous108532114
1213893356213893357AT14GENIChomozygous108532116
1213893368213893369GC15GENIChomozygous108532117
1213893489213893490GA19GENIChomozygous108532118
1213893561213893562CT18GENIChomozygous108532119
1213893641213893642AG18GENIChomozygous108532120
1213894158213894159GC20GENIChomozygous108532121
1213894229213894232CTT17GENIChomozygous127481042
1213894282213894283TC16GENIChomozygous108532122
1213894527213894528AG12GENIChomozygous108532123
1213895174213895174G16GENIChomozygous127481043
1213895413213895419CAGAGG21GENIChomozygous127481044
1213895761213895762TC19GENIChomozygous108532124
1213896124213896125GA16GENIChomozygous108532125
1213896806213896807CT17GENIChomozygous108532126
1213897523213897523C8GENIChomozygous127481045
1213897567213897568CT6GENIChomozygous109366979
1213897637213897637TGAC11GENIChomozygous127481046