chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110470979110470980AG38GENIChomozygous116720734
10110471865110471866GA34GENIChomozygous116720736
10110474643110474644TC41GENIChomozygous116720738
10110474870110474871GA51GENIChomozygous116720740
10110475466110475467AG57GENIChomozygous116720742
10110476387110476388AG37GENICpossibly homozygous116720744
10110477076110477077AG40GENIChomozygous116720746
10110477142110477143TA43GENIChomozygous116720748
10110477783110477784GA38GENIChomozygous116720750
10110479774110479775AG39GENIChomozygous116720752
10110481191110481192AG33GENIChomozygous116720754
10110482465110482466GA29GENIChomozygous116720756
10110483535110483536AG27GENIChomozygous116720758
10110483823110483824CT43GENIChomozygous116720760
10110484557110484558CG70GENIChomozygous116720762
10110484661110484662GA53GENIChomozygous116720764
10110484877110484878AG34GENIChomozygous116720766
10110486291110486292TA19GENIChomozygous116720772
10110485254110485255GA10GENIChomozygous116720768
10110485965110485966AG36GENIChomozygous116720770
10110487034110487035CA42GENIChomozygous116720774
10110488054110488055CT26GENIChomozygous116720776
10110488587110488588GA52GENIChomozygous116720778
10110489420110489421AG37GENIChomozygous116720780
10110489523110489524TC59GENIChomozygous116720782
10110490726110490727GA43GENIChomozygous116720784
10110493415110493416GT39GENIChomozygous116720786
10110495040110495041GA66GENIChomozygous116720788
10110497633110497634GA44GENIChomozygous116720790
10110497668110497669AG45GENIChomozygous116720792
10110498831110498832AG29GENIChomozygous116720794
10110498842110498843CT27GENIChomozygous116720796
10110500749110500750GT30GENIChomozygous116720798
10110505606110505607GT37GENIChomozygous116720800
10110505608110505609TC37GENIChomozygous116720802
10110510213110510214GA43GENIChomozygous116720804
10110511067110511068AG47GENIChomozygous116720806
10110513563110513564CA33GENIChomozygous116720808
10110514549110514550AT47GENIChomozygous116720810