chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671498366714984CT18GENIChomozygous947803906
116671525366715254CT29GENIChomozygous947803907
116671589766715898GA39GENIChomozygous947803908
116671647966716480TC21GENIChomozygous947803909
116671668466716685GA22GENIChomozygous947803910
116671728366717284AT13GENIChomozygous947803911
116671730866717309TA9GENIChomozygous947803912
116671755366717554CA15GENIChomozygous947803913
116671760366717604GC19GENIChomozygous947803914
116671886666718867AG30GENIChomozygous947803915
116671969366719694TA15GENIChomozygous947803916
116671989366719894GA19GENIChomozygous947803917
116671991266719913GT23GENIChomozygous947803918
116672055666720557AG28GENIChomozygous947803919
116672164466721645TC21GENIChomozygous947803920
116672350966723510TC24GENIChomozygous947803921
116672411266724113AC20GENIChomozygous947803922
116672422866724229TC26GENIChomozygous947803923
116672543466725435TC27GENIChomozygous947803924
116672636166726362TC25GENIChomozygous947803925
116672675466726755GC21GENIChomozygous947803926
116672734666727347AG31GENIChomozygous947803927
116672886966728870AC12GENICheterozygous947803928
116672959066729591AT23GENIChomozygous947803929
116673084166730842GA17GENIChomozygous947803930