chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16650430266504306AAAC----26GENIChomozygous62683708
16650575966505760TC18GENICpossibly homozygous62077419
16650580366505804TC17GENIChomozygous61996712
16650629266506293AG10GENIChomozygous62077420
16650640366506404TTG5GENIChomozygous62077421
16650673266506733CT14GENIChomozygous61996716
16650759266507593TTTGA20GENIChomozygous61996717
16650759466507595AAG19GENIChomozygous61996718
16650822766508228CT18GENIChomozygous62444603
16650921866509219TC18GENIChomozygous61996721
16650974466509745AG17GENIChomozygous62077422
16651037266510373TTC22GENIChomozygous61996723
16651039466510395GC18GENIChomozygous62077423
16651084166510842GA17GENIChomozygous62077424
16651140666511407CT23GENIChomozygous62077425
16651146866511469GGT8GENICheterozygous62244944
16651209066512091GA29GENIChomozygous61996727
16651250566512506AG29GENIChomozygous61996728
16651269566512696AG26GENIChomozygous62077426
16651397066513971CCT33GENIChomozygous62683709
16651468366514684CT19GENIChomozygous62077427
16651646566516466GC7GENIChomozygous61996731
16650652366506524T-10GENIChomozygous60733845
16650759066507591TTCTGAAGAC19GENIChomozygous61950212