chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246991714699172TTAGACAA11GENIChomozygous50004803
1246991874699188GC14GENIChomozygous50004807
1246994414699442AG18GENIChomozygous50004815
1246995524699553GA21GENIChomozygous50004817
1246996894699690CT22GENIChomozygous50394995
1246998834699884GA11GENIChomozygous50004819
1247009334700934GA7GENIChomozygous50004821
1247011934701194AT13GENIChomozygous50004823
1247012194701220GA11GENIChomozygous50004825
1247012984701299CT20GENIChomozygous50004827
1247014094701410GA11GENIChomozygous50004829
1247024164702417CT10GENIChomozygous50004831
1247026764702677GA18GENIChomozygous50004833
1247040184704019TC15GENIChomozygous50394997
1247040334704034TC14GENIChomozygous50394999
1247040584704059TTAA7GENICheterozygous50004835
1247040584704059TTA7GENICheterozygous50606370
1247041344704135CT12GENIChomozygous50395001
1247042834704284TC13GENIChomozygous50395003
1247058064705807CT20GENIChomozygous50395007
1247059794705980TTACACAC2GENIChomozygous50526690
1247061914706192GGAAA13GENICheterozygous50567226
1247069494706950AG19GENIChomozygous50004849
1247077704707771GGCC2GENIChomozygous50526692
1247077744707775GGC2GENIChomozygous50526694
1247077754707776GGCGCCC2GENIChomozygous50526696
1247080314708032CT1GENIChomozygous50395009