chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123492513123492514TC3GENIChomozygous56172331
7123492810123492826CCATCCATCCATCCAT----------------10GENIChomozygous55767967
7123493663123493664TC26GENIChomozygous54090077
7123493962123493963CT32GENIChomozygous56172333
7123493987123493988AG37GENIChomozygous54090078
7123494480123494481TG32GENICpossibly homozygous56172335
7123494616123494617TA27GENICpossibly homozygous54090079
7123496050123496051GT23GENICpossibly homozygous56172337
7123496194123496195AG23GENIChomozygous54236411
7123496363123496364CT35GENIChomozygous56172339
7123496992123496993AG22GENIChomozygous54236413
7123497091123497092TC32GENIChomozygous54090083
7123497135123497136TC29GENIChomozygous54236417
7123497427123497428GA25GENIChomozygous56172341
7123497448123497449TC27GENICpossibly homozygous54090084
7123497628123497629GGA19GENICheterozygous54090085
7123497628123497629GGAA19GENICpossibly homozygous55144972
7123497927123497930ACC---30GENIChomozygous54090086
7123497969123497972CAT---32GENIChomozygous56172343
7123497979123497980CT35GENIChomozygous56172345
7123498212123498213CT47GENIChomozygous54236421
7123498828123498829CT31GENIChomozygous56172347
7123501483123501484GT29GENIChomozygous56172349
7123501751123501752AG22GENIChomozygous54090096
7123504305123504306AAACACACAC11GENIChomozygous56109420
7123504556123504557TTAC23GENIChomozygous54921458
7123504617123504618TTACACAC17GENIChomozygous54090109
7123504899123504901AC--12GENIChomozygous55030561
7123505848123505849TC23GENIChomozygous56172351
7123506772123506773CT13GENIChomozygous56172353
7123506859123506860CT26GENIChomozygous56172355
7123507836123507837TC10GENIChomozygous54090141
7123508894123508896GT--7GENICpossibly homozygous55144975
7123510427123510428GA27GENIChomozygous56172357
7123510735123510751AGAGAGAGAGAGAGAG----------------13GENICheterozygous56172359
7123510737123510751AGAGAGAGAGAGAG--------------13GENICheterozygous56172361
7123510784123510785GT29GENIChomozygous56172363