chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109014044390140444GT38GENICheterozygous51735957
109014045090140451TG36GENICheterozygous51735959
109014047390140474GA39GENICheterozygous51735961
109014052690140527TC50GENICheterozygous51735964
109014140490141405AT37GENIChomozygous51735968
109014178990141790TC33GENIChomozygous51735970
109014183190141832T-20GENIChomozygous51537752
109014271790142718A-3GENIChomozygous51735972
109014291190142912CT44GENIChomozygous51735974
109014360690143607AG34GENIChomozygous51735976
109014432390144324TC23GENIChomozygous51735978
109014535090145351CCT5INTERGENIChomozygous51735980
109014570790145708C-25INTERGENIChomozygous51537755
109014787290147873GA27INTERGENIChomozygous51735982
109014816290148163CT26INTERGENIChomozygous51537757
109014835590148357CA--31INTERGENIChomozygous51537758
109014848990148490CCGT18INTERGENICpossibly homozygous51537759
109014874390148744CCT9INTERGENICpossibly homozygous51537762
109014994290149943CT45INTERGENIChomozygous51735984
109015216990152170TTATAA1INTERGENIChomozygous51537765
109015239090152394TTCT----33INTERGENIChomozygous51537766
109015250390152504CT43INTERGENIChomozygous51735986
109015384890153849GGA10INTERGENICheterozygous51537769
109015455990154560AT15INTERGENIChomozygous51537771
109015528490155285CT45INTERGENIChomozygous51537773
109015582290155823AAG18INTERGENICheterozygous51735988
109015644090156441GGAA11INTERGENIChomozygous51735990
109015783390157834AG33INTERGENIChomozygous51537778
109015796290157963TTCA9INTERGENIChomozygous51735992
109015800990158011CT--24INTERGENICpossibly homozygous51537779
109015870590158706AATT9INTERGENIChomozygous51537781
109015988690159887TTA19INTERGENIChomozygous51735994
109016130590161306CCAA29INTERGENIChomozygous51735998
109016162590161629AAAA----9INTERGENICpossibly homozygous51736000
109016163990161640AAG15INTERGENICheterozygous51537789
109016347790163478AG48INTERGENIChomozygous51537791
109016457890164579AAC30INTERGENIChomozygous51537794
109016537990165380CT22INTERGENIChomozygous51736002
109016585290165853TTC10GENICpossibly homozygous51537795
109016586190165862TTTG10GENIChomozygous51537796
109016644790166448AAT19GENICpossibly homozygous51537797
109016739590167396GA32GENIChomozygous51736004
109016797990167980CT39GENIChomozygous51537798
109016857790168578TC37GENIChomozygous51537799