chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101860283618602837GA26GENIChomozygous116740676
101860355118603552TC29GENIChomozygous116503475
101860370718603708AG20GENIChomozygous116503477
101860370918603710TC19GENIChomozygous116503479
101860378518603786GA32GENIChomozygous116503481
101860387618603877GA26GENIChomozygous116503483
101860434218604343TC23GENIChomozygous116503485
101860444218604443GT35GENIChomozygous116503487
101860482918604830GA26GENICpossibly homozygous116740677
101860507318605074GA29GENIChomozygous116503489
101860591918605920GA20GENIChomozygous116503491
101860665218606653CT28GENIChomozygous116503493
101860790318607904AG33GENIChomozygous116503497
101860900618609007GA37GENIChomozygous116740678
101860917118609172TC26GENIChomozygous116503503