chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246991714699172TTAGACAA23GENIChomozygous50004803
1246991814699182CCA25GENICpossibly homozygous50004805
1246991874699188GC17GENIChomozygous50004807
1246991874699188GA11GENIChomozygous50004809
1246991904699191AAC26GENICheterozygous50004811
1246994414699442AG29GENIChomozygous50004815
1246995524699553GA26GENIChomozygous50004817
1246996894699690CT27GENIChomozygous50394995
1246998834699884GA32GENIChomozygous50004819
1247009334700934GA24GENIChomozygous50004821
1247011934701194AT23GENIChomozygous50004823
1247012194701220GA17GENIChomozygous50004825
1247012984701299CT26GENIChomozygous50004827
1247014094701410GA46GENIChomozygous50004829
1247024164702417CT33GENIChomozygous50004831
1247026764702677GA38GENIChomozygous50004833
1247040184704019TC8GENICpossibly homozygous50394997
1247040334704034TC7GENICpossibly homozygous50394999
1247040594704060A-4GENICheterozygous50274692
1247041344704135CT24GENIChomozygous50395001
1247042834704284TC35GENIChomozygous50395003
1247046844704685TC43GENIChomozygous50395005
1247058064705807CT21GENIChomozygous50395007
1247069494706950AG24GENIChomozygous50004849
1247077714707772AC3GENIChomozygous50004855
1247077744707775GC3GENIChomozygous50004859
1247077754707776GC3GENIChomozygous50004861
1247080314708032CT30GENIChomozygous50395009