chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105432864054328641GA24GENIChomozygous116600094
105432882954328830TC16GENIChomozygous116600096
105432891654328917GC9GENIChomozygous116600098
105433073254330733GA25GENIChomozygous116600100
105433117454331175GA11GENIChomozygous116600102
105433193754331938CT23GENIChomozygous116600104
105433206554332066GC12GENIChomozygous116600106
105433234454332345AG12GENIChomozygous116600108
105433492154334922AT15GENIChomozygous116600112
105433499454334995AG17GENIChomozygous116600114
105433510054335101CT16GENIChomozygous116600116
105433533854335339AG15GENIChomozygous116600118
105433602854336029GC19GENIChomozygous116600120
105433695654336957TG19GENIChomozygous116600122
105433775254337753GT17GENIChomozygous116600124
105433787054337871GT16GENIChomozygous116600126
105433829954338300AG19GENIChomozygous116600128
105433857554338576CA14GENIChomozygous116600130
105433937354339374CT14GENIChomozygous116600132
105434030054340301GT21GENIChomozygous116600134
105434106254341063AG18GENIChomozygous116600136
105434106754341068TA16GENIChomozygous116600138
105434112354341124GA15GENIChomozygous116600140
105434194454341945CT31GENIChomozygous116600142
105434267554342676CT10GENIChomozygous116600144
105433980054339801TA9GENICheterozygous117218716
105433980254339803AT9GENICheterozygous117218718