chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105958711059587111CT23GENIChomozygous51465833
105958767859587679CT11GENIChomozygous51465834
105958976759589768TC15GENIChomozygous51465835
105959129359591300GGCATTT-------10GENIChomozygous51465836
105959390759593908TC30GENICpossibly homozygous51465837
105959928459599285GT27GENICpossibly homozygous51465839
105960012859600129G-7GENIChomozygous51465841
105960068259600683GGTT2GENICheterozygous51465843
105960650559606506CT17GENIChomozygous51465846