chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461753876175388AG14GENIChomozygous962075590
1461753886175389GA15GENIChomozygous962075591
1461767686176769AT24GENIChomozygous962075592
1461771496177150TC31GENIChomozygous962075593
1461774006177401GC24GENIChomozygous962075594
1461774566177457TC22GENIChomozygous962075595
1461775596177560AG37GENIChomozygous962075596
1461776266177627AG22GENIChomozygous962075597
1461778266177827AG25GENIChomozygous962075598
1461811396181140GA24GENIChomozygous962075599
1462189296218930CT19GENIChomozygous962075600
1462193116219312CT27GENIChomozygous962075601
1462194456219446GA36GENICpossibly homozygous962075602
1462196006219601GA33GENIChomozygous962075603
1462202146220215CG18GENIChomozygous962075604
1462202236220224CT16GENIChomozygous962075605
1462204066220407GA12GENIChomozygous962075606
1462207146220715AG19GENIChomozygous962075607
1462209816220982AG25GENIChomozygous962075608
1462212306221231TC19GENIChomozygous962075609