chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123857553938575540T-9GENICpossibly homozygous50194768
123857881138578812AG33GENIChomozygous50194770
123858093238580933TTAGAGAG15GENICheterozygous50194772
123858164638581647A-12GENICheterozygous50194774
123858585638585857CCT8GENICheterozygous50412770
123858593038585931A-1GENIChomozygous50194776
123858594938585950AAGC1GENIChomozygous50194778
123859532038595321CCTGG3GENIChomozygous50194780
123859532338595324CCTTGA1GENIChomozygous50194782
123859632538596326AAATAG14GENIChomozygous50194784
123859801538598016TTAC21GENICheterozygous50194786
123859801538598016TTACAC21GENICpossibly homozygous50194788
123859822738598228A-10GENICheterozygous50322790
123860502938605033TATA----6GENIChomozygous50194790
123860709138607092C-22GENICheterozygous50194794
123860883038608831C-2GENIChomozygous50194796
123861487238614873AC17GENICheterozygous50194802
123861801238618013TC9GENICheterozygous50450974
123862447338624474CT28GENICheterozygous50322798