chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246991714699172TTAGACAA18GENIChomozygous50004803
1246991874699188GC19GENIChomozygous50004807
1246994414699442AG21GENIChomozygous50004815
1246995524699553GA28GENIChomozygous50004817
1246996894699690CT31GENIChomozygous50394995
1246998834699884GA22GENIChomozygous50004819
1247009334700934GA9GENIChomozygous50004821
1247011934701194AT5GENIChomozygous50004823
1247012194701220GA6GENIChomozygous50004825
1247012984701299CT14GENIChomozygous50004827
1247014094701410GA14GENIChomozygous50004829
1247024164702417CT17GENIChomozygous50004831
1247026764702677GA11GENIChomozygous50004833
1247040184704019TC14GENIChomozygous50394997
1247040334704034TC12GENIChomozygous50394999
1247040584704059TTAA7GENICheterozygous50004835
1247040584704059TTA7GENICheterozygous50606370
1247041344704135CT21GENIChomozygous50395001
1247042834704284TC18GENIChomozygous50395003
1247058064705807CT19GENIChomozygous50395007
1247059794705980TTAC6GENICheterozygous50555893
1247059794705980TTACACACAC6GENICheterozygous50567225
1247069494706950AG21GENIChomozygous50004849
1247080314708032CT3GENIChomozygous50395009
1247059794705980TTACACAC6GENICheterozygous50526690
1247077704707771GGCC3GENIChomozygous50526692
1247077744707775GGC3GENIChomozygous50526694
1247077754707776GGCGCCC3GENIChomozygous50526696