chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1050023685002369TG16GENIChomozygous944577904
1050026765002677AG35GENIChomozygous944577905
1050030225003023TC36GENIChomozygous944577906
1050030945003095GA23GENIChomozygous944577907
1050034525003453GA42GENIChomozygous944577908
1050104695010470CA26GENIChomozygous944577909
1050104805010481TC33GENIChomozygous944577910
1050128695012870CT29GENIChomozygous944577911
1050141935014194CT21GENIChomozygous944577912
1050154265015427GA22GENIChomozygous944577913
1050170515017052CT35GENIChomozygous944577914
1050184585018459CT25GENIChomozygous944577915
1050221635022164CT47GENIChomozygous944577916
1050225175022518GA26GENIChomozygous944577917
1050234125023413AG31GENIChomozygous944577918
1050236885023689AG37GENIChomozygous944577919
1050242825024283AG34GENIChomozygous944577920
1050244685024469TA21GENIChomozygous944577921
1050245615024562AT20GENIChomozygous944577922
1050246735024674AC30GENIChomozygous944577923
1050265515026552TC29GENIChomozygous944577924
1050346305034631GA27GENIChomozygous944577925
1050398645039865AG23GENIChomozygous944577926
1050398655039866TA25GENIChomozygous944577927
1050403345040335TC27GENIChomozygous944577928
1050405625040563GA22GENIChomozygous944577929
1050409295040930GC29GENIChomozygous944577930
1050423765042377CT37GENIChomozygous944577931
1050423855042386TA40GENIChomozygous944577932
1050960335096034CA38GENIChomozygous944577933
1050960465096047AT34GENIChomozygous944577934
1050961795096180CT24GENIChomozygous944577935
1050961815096182CA26GENIChomozygous944577936
1050968535096854CT18GENIChomozygous944577937
1051031795103180TC33GENIChomozygous944577938
1051032205103221TC29GENIChomozygous944577939
1051106365110637TA36GENIChomozygous944577940
1051134305113431TC26GENIChomozygous944577941
1051703145170315CT29GENIChomozygous944577942
1051852735185274GA44GENIChomozygous944577943
1051883535188354AG29GENIChomozygous944577944
1051889095188910CT41GENIChomozygous944577945