chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141865303218653033AAT22GENIChomozygous48552770
141865307818653079TG32GENIChomozygous48552771
141865389018653891AT36GENIChomozygous48552772
141865389118653892AC37GENICpossibly homozygous48552773
141865399118653992TC51GENIChomozygous48552774
141865405918654060CT59GENICpossibly homozygous48961011
141865414918654150TC57GENIChomozygous48552775