chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246991714699172TTAGACAA13GENIChomozygous50004803
1246991874699188GC13GENIChomozygous50004807
1246994374699438CA14GENIChomozygous50004813
1246994414699442AG15GENIChomozygous50004815
1246995524699553GA29GENIChomozygous50004817
1246998834699884GA18GENIChomozygous50004819
1247009334700934GA8GENIChomozygous50004821
1247011934701194AT14GENIChomozygous50004823
1247012194701220GA14GENIChomozygous50004825
1247012984701299CT19GENIChomozygous50004827
1247014094701410GA18GENIChomozygous50004829
1247024164702417CT11GENIChomozygous50004831
1247026764702677GA12GENIChomozygous50004833
1247040584704059TTAA2GENIChomozygous50004835
1247056734705674CA16GENIChomozygous50004839
1247057604705761TC19GENIChomozygous50004841
1247059804705986ACACAC------10GENIChomozygous50004843
1247061914706192GGA11GENICheterozygous50004847
1247069494706950AG29GENIChomozygous50004849
1247073804707381GT15GENIChomozygous50004851
1247075594707560AG10GENIChomozygous50004853
1247077704707771GGCC4GENIChomozygous50526692
1247077744707775GGC4GENIChomozygous50526694
1247077754707776GGCGCCC4GENIChomozygous50526696