chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105958711059587111CT19GENICpossibly homozygous51465833
105958767859587679CT14GENIChomozygous51465834
105959390759593908TC24GENIChomozygous51465837
105959928459599285GT20GENIChomozygous51465839
105960012859600129G-12GENIChomozygous51465841
105960650559606506CT21GENIChomozygous51465846