chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123809583538095836AC61GENIChomozygous781807993
123809997938099980GA61GENICpossibly homozygous781807994
123810097338100974GC52GENIChomozygous781807995
123810111338101114GA39GENICpossibly homozygous781807996
123810112338101124GT32GENIChomozygous781807997
123810441738104418AT46GENIChomozygous781807998
123811057838110579AG58GENIChomozygous781807999
123811271138112712GA76GENICpossibly homozygous781808000
123811392338113924GC37GENIChomozygous781808001
123811394538113946TC32GENIChomozygous781808002
123811397738113978GA18GENIChomozygous781808003
123811725638117257GA49GENIChomozygous781808004