chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205563681205563682TC21GENIChomozygous61064987
1205563707205563708CT26GENIChomozygous61064988
1205563735205563736TG25GENIChomozygous61064989
1205563871205563872CT15GENIChomozygous61064990
1205564578205564579CT15GENIChomozygous61064991
1205564854205564855CT21GENIChomozygous61064992
1205565159205565160GA19GENIChomozygous61064993
1205565251205565252TC18GENIChomozygous61064994
1205566161205566162CT17GENIChomozygous61064995
1205566319205566320GA21GENIChomozygous61064996
1205567843205567844AC9GENIChomozygous61064997
1205568449205568458CTCAGTTCC---------12GENIChomozygous61064999
1205569044205569045CT23GENICheterozygous61065003
1205569053205569054CT21GENICheterozygous62804045
1205569136205569139GGG---15GENIChomozygous62030282
1205569139205569140TC15GENIChomozygous62236215
1205569489205569490T-21GENIChomozygous61065004
1205569882205569884TG--18GENIChomozygous61065006
1205569965205569966AC24GENIChomozygous61065008
1205570746205570747GA20GENIChomozygous62030283
1205571578205571579GA9GENIChomozygous61065014
1205571835205571836AG10GENIChomozygous62030285
1205571856205571862CATACA------7GENIChomozygous62030286
1205572616205572617TC22GENIChomozygous61065017
1205572857205572870GAGAAACAAAACA-------------12GENIChomozygous62030287
1205573002205573003AAT22GENIChomozygous61065018
1205573119205573120GT15GENIChomozygous62030288
1205573173205573174T-13GENIChomozygous62030289
1205573193205573194CT19GENIChomozygous62030290
1205573502205573503GA14GENIChomozygous61065019
1205574466205574467TC26GENIChomozygous61065023
1205575438205575439TTAAGAAA10GENIChomozygous61065027
1205575486205575487AG19GENIChomozygous61065028
1205576238205576239GC19GENIChomozygous61065029