chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123492513123492514TC3GENIChomozygous645255778
7123492810123492826CCATCCATCCATCCAT----------------10GENIChomozygous754226665
7123493663123493664TC26GENIChomozygous645255779
7123493962123493963CT32GENIChomozygous645255780
7123493987123493988AG37GENIChomozygous645255781
7123494480123494481TG32GENICpossibly homozygous645255782
7123494616123494617TA27GENICpossibly homozygous645255783
7123496050123496051GT23GENICpossibly homozygous645255784
7123496194123496195AG23GENIChomozygous645255785
7123496363123496364CT35GENIChomozygous645255786
7123496992123496993AG22GENIChomozygous645255787
7123497091123497092TC32GENIChomozygous645255788
7123497135123497136TC29GENIChomozygous645255789
7123497427123497428GA25GENIChomozygous645255790
7123497448123497449TC27GENICpossibly homozygous645255791
7123497628123497629GGA19GENICheterozygous754226669
7123497628123497629GGAA19GENICpossibly homozygous754226670
7123497927123497930ACC---30GENIChomozygous754226671
7123497969123497972CAT---32GENIChomozygous754226672
7123497979123497980CT35GENIChomozygous645255792
7123498212123498213CT47GENIChomozygous645255793
7123498828123498829CT31GENIChomozygous645255794
7123501483123501484GT29GENIChomozygous645255795
7123501751123501752AG22GENIChomozygous645255796
7123504305123504306AAACACACAC11GENIChomozygous754226674
7123504556123504557TTAC23GENIChomozygous754226676
7123504617123504618TTACACAC17GENIChomozygous754226680
7123504899123504901AC--12GENIChomozygous754226681
7123505848123505849TC23GENIChomozygous645255797
7123506772123506773CT13GENIChomozygous645255798
7123506859123506860CT26GENIChomozygous645255799
7123507836123507837TC10GENIChomozygous645255800
7123508894123508896GT--7GENICpossibly homozygous754226685
7123510427123510428GA27GENIChomozygous645255801
7123510735123510751AGAGAGAGAGAGAGAG----------------13GENICheterozygous754226688
7123510737123510751AGAGAGAGAGAGAG--------------13GENICheterozygous754226689
7123510784123510785GT29GENIChomozygous645255802