chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261483933261483934AG26GENIChomozygous120881365
1261484479261484480TA13GENIChomozygous109216027
1261485253261485254CT27GENIChomozygous120881366
1261485581261485582CT15GENIChomozygous109216029
1261485677261485678GA10GENIChomozygous109216031
1261486336261486337TC15GENIChomozygous109216033
1261486473261486474TC19GENIChomozygous109216035
1261486943261486944TC19GENIChomozygous109216037
1261486964261486965TC20GENIChomozygous109216039
1261486965261486966AG21GENIChomozygous109216041
1261487633261487634CA16GENIChomozygous109216047
1261488121261488122GC32GENIChomozygous109216049
1261488443261488444GA22GENIChomozygous109216051
1261488826261488827AG22GENIChomozygous109216053
1261488874261488875GA26GENIChomozygous109216055
1261489178261489179TC12GENIChomozygous109216057
1261489228261489229GA11GENIChomozygous109216059
1261489366261489367TC15GENIChomozygous109216063
1261489532261489533TA20GENIChomozygous109216065
1261489596261489597CT20GENIChomozygous109216067
1261490089261490090GA21GENIChomozygous109216069
1261490113261490114CT20GENIChomozygous109216071
1261490170261490171TA19GENIChomozygous109216073
1261490218261490219CT19GENIChomozygous109216075
1261490307261490308TC18GENIChomozygous109216077
1261490623261490624CG22GENIChomozygous109216079
1261490714261490715TC26GENIChomozygous109216081
1261490929261490930AG26GENIChomozygous109216085
1261491034261491035TC27GENIChomozygous109216087
1261491244261491245TC24GENIChomozygous109216089
1261491379261491380TC19GENIChomozygous109216091
1261491463261491464TC19GENIChomozygous109216093
1261491677261491678CG23GENIChomozygous109216095
1261492263261492264GA20GENIChomozygous109216099
1261492297261492298AG29GENIChomozygous109216101
1261492631261492632AG21GENIChomozygous109216103
1261493549261493550TA19GENIChomozygous109216107
1261494160261494161CG14GENIChomozygous109216109
1261494317261494318GA24GENIChomozygous109216111
1261494323261494324AC24GENIChomozygous109216113