chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85912314759123148CT19GENIChomozygous116511053
85912315359123154CA18GENICpossibly homozygous116511055
85912318859123189TC15GENICpossibly homozygous116511057
85912319359123194TC17GENICpossibly homozygous116511059
85912352159123522AG21GENICpossibly homozygous116511061
85912387159123872TC17GENICpossibly homozygous116511063
85912440959124410TC30GENICpossibly homozygous118145755
85912456359124564TC31GENICpossibly homozygous116511065
85912461559124616GA35GENICpossibly homozygous116511067
85912523859125239AG26GENIChomozygous116511069
85912797659127977TG27GENIChomozygous117184666
85912804659128047GA25GENICpossibly homozygous117184667
85913217559132176GA17GENIChomozygous116511087
85913338759133388AG22GENIChomozygous116511089
85913366559133666TC17GENIChomozygous116511091
85913387759133878CT30GENICpossibly homozygous117184668
85913496259134963GA20GENICpossibly homozygous118145757
85913740759137408GA33GENICpossibly homozygous118145759