chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246991714699172TTAGACAA13GENIChomozygous50004803
1246991874699188GC16GENIChomozygous50004807
1246994414699442AG19GENIChomozygous50004815
1246995524699553GA16GENIChomozygous50004817
1246996894699690CT20GENIChomozygous50394995
1246998834699884GA12GENIChomozygous50004819
1247009334700934GA7GENIChomozygous50004821
1247011934701194AT4GENIChomozygous50004823
1247012194701220GA4GENIChomozygous50004825
1247012984701299CT14GENIChomozygous50004827
1247014094701410GA10GENIChomozygous50004829
1247024164702417CT12GENIChomozygous50004831
1247026764702677GA7GENIChomozygous50004833
1247040184704019TC11GENIChomozygous50394997
1247040334704034TC8GENIChomozygous50394999
1247040584704059TTA2GENICheterozygous50606370
1247041344704135CT9GENICpossibly homozygous50395001
1247042834704284TC9GENIChomozygous50395003
1247058064705807CT14GENIChomozygous50395007
1247059794705980TTAC3GENICheterozygous50555893
1247069494706950AG24GENIChomozygous50004849
1247077754707776GGCGCCC3GENIChomozygous50526696
1247059794705980TTACACAC3GENICheterozygous50526690
1247077704707771GGCC3GENIChomozygous50526692
1247077744707775GGC3GENIChomozygous50526694
1247080314708032CT3GENIChomozygous50395009