chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261483933261483934AG12GENIChomozygous120881365
1261485253261485254CT23GENIChomozygous120881366
1261485581261485582CT25GENIChomozygous109216029
1261485677261485678GA16GENIChomozygous109216031
1261486473261486474TC16GENIChomozygous109216035
1261486943261486944TC15GENIChomozygous109216037
1261486964261486965TC11GENIChomozygous109216039
1261486965261486966AG12GENIChomozygous109216041
1261488121261488122GC16GENIChomozygous109216049
1261488443261488444GA26GENIChomozygous109216051
1261488826261488827AG27GENIChomozygous109216053
1261488874261488875GA19GENIChomozygous109216055
1261489178261489179TC20GENIChomozygous109216057
1261489228261489229GA14GENIChomozygous109216059
1261489366261489367TC20GENIChomozygous109216063
1261489532261489533TA15GENIChomozygous109216065
1261489596261489597CT13GENIChomozygous109216067
1261490089261490090GA16GENIChomozygous109216069
1261490218261490219CT21GENIChomozygous109216075
1261490307261490308TC23GENIChomozygous109216077
1261490623261490624CG26GENIChomozygous109216079
1261490714261490715TC16GENIChomozygous109216081
1261490929261490930AG19GENIChomozygous109216085
1261491034261491035TC21GENIChomozygous109216087
1261491244261491245TC11GENIChomozygous109216089
1261491379261491380TC18GENIChomozygous109216091
1261491463261491464TC30GENIChomozygous109216093
1261491677261491678CG14GENIChomozygous109216095
1261492263261492264GA27GENIChomozygous109216099
1261492297261492298AG33GENIChomozygous109216101
1261492631261492632AG23GENIChomozygous109216103
1261493549261493550TA6GENIChomozygous109216107
1261494160261494161CG19GENIChomozygous109216109
1261494317261494318GA28GENIChomozygous109216111
1261494323261494324AC32GENIChomozygous109216113