chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X121054277121054278TA16GENIChomozygous108421929
X121054859121054860GA9GENIChomozygous108320945
X121055961121055962TC17GENICpossibly homozygous119950019
X121056050121056051AG89GENICheterozygous120010895
X121056101121056102GA57GENICheterozygous120010896
X121057930121057931AG4GENIChomozygous108320948
X121058118121058119TG5GENIChomozygous108421931
X121058358121058359GA3GENIChomozygous108421933
X121058804121058805CT10GENIChomozygous108421935
X121060021121060022CT16GENIChomozygous108421937
X121060320121060321AG9GENIChomozygous108320950
X121060580121060581TG9GENIChomozygous108421939
X121062272121062273AG9GENIChomozygous108421941
X121062759121062760TC9GENIChomozygous108421943
X121063891121063892GT12GENIChomozygous108421945
X121063973121063974TC11GENIChomozygous108421947
X121064461121064462CT8GENIChomozygous108421949
X121064512121064513GT8GENIChomozygous108421951
X121064763121064764TC11GENIChomozygous108421953
X121064776121064777TC9GENIChomozygous108320954
X121065193121065194CT15GENIChomozygous108421955
X121065399121065400AG11GENIChomozygous108320956
X121066144121066145CT7GENIChomozygous108320958
X121066216121066217GA9GENIChomozygous108421959
X121066307121066308TC9GENIChomozygous108320960
X121066518121066519AG15GENIChomozygous108320964
X121066524121066525CT15GENIChomozygous108421961
X121066621121066622GT9GENIChomozygous108421963
X121066672121066673CA12GENIChomozygous108421965
X121056674121056675GT13GENIChomozygous120060604
X121057209121057210GA9GENICheterozygous120107282