chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205563707205563708CT18GENICpossibly homozygous61064988
1205563735205563736TG15GENIChomozygous61064989
1205563871205563872CT8GENIChomozygous61064990
1205564578205564579CT24GENIChomozygous61064991
1205564654205564655GC12GENIChomozygous62694926
1205564805205564806CT23GENIChomozygous62694927
1205564854205564855CT15GENIChomozygous61064992
1205565251205565252TC15GENIChomozygous61064994
1205566010205566011CT6GENIChomozygous62694928
1205566161205566162CT26GENICpossibly homozygous61064995
1205566319205566320GA7GENIChomozygous61064996
1205566799205566800CG12GENICpossibly homozygous62694929
1205567843205567844AC3GENIChomozygous61064997
1205568336205568337C-4GENIChomozygous61682525
1205568449205568458CTCAGTTCC---------2GENIChomozygous61064999
1205569882205569884TG--7GENIChomozygous61065006
1205569965205569966AC15GENICpossibly homozygous61065008
1205570400205570401TC18GENICpossibly homozygous61065009
1205571132205571133CCA12GENICpossibly homozygous62030284
1205571578205571579GA4GENIChomozygous61065014
1205571835205571836AG11GENIChomozygous62030285
1205571856205571862CATACA------1GENIChomozygous62030286
1205572616205572617TC6GENIChomozygous61065017
1205572857205572870GAGAAACAAAACA-------------2GENIChomozygous62030287
1205573002205573003AAT15GENIChomozygous61065018
1205573119205573120GT9GENIChomozygous62030288
1205573173205573174T-16GENIChomozygous62030289
1205573193205573194CT14GENIChomozygous62030290
1205573502205573503GA13GENIChomozygous61065019
1205574466205574467TC6GENIChomozygous61065023
1205575454205575455AAAAAAG2GENICheterozygous62694930
1205575486205575487AG10GENIChomozygous61065028
1205576238205576239GC14GENIChomozygous61065029