chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136780802567808026CT43GENIChomozygous66076601
136780867367808674CT24GENIChomozygous66076604
136780893867808939CT54GENIChomozygous66076607
136780962067809621TC18GENIChomozygous66076610
136780991067809911AG37GENIChomozygous66076613
136781009467810095GA54GENIChomozygous66076615
136781120367811204GT7GENIChomozygous66076618
136781121267811213GT10GENIChomozygous66076621
136781123767811238AG12GENIChomozygous66076624
136781358667813587TC35GENIChomozygous66076627
136781675067816751CT17GENIChomozygous66076630
136781876167818762CG47GENIChomozygous66076633
136782257667822577TC54GENIChomozygous66076636
136782273767822738TC55GENIChomozygous66076639
136782299567822996AG65GENIChomozygous66076641
136782304667823047AC56GENIChomozygous66076644
136782304767823048GT56GENIChomozygous66076647
136782524567825246AT33GENIChomozygous66076650
136782574767825748GA39GENIChomozygous66076653
136782604967826050GA52GENIChomozygous66076656
136782650767826508AG37GENIChomozygous66076659
136782868367828684TC56GENIChomozygous66076664
136782945667829457GA37GENIChomozygous66076667
136782976967829770CA31GENIChomozygous66076670
136783005967830060CT29GENIChomozygous66076673
136783152967831530AG45GENIChomozygous66076676
136783270167832702GT51GENIChomozygous66076682
136783270367832704GT52GENICpossibly homozygous66076685