chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105958711059587111CT16GENICpossibly homozygous51465833
105958767859587679CT18GENICpossibly homozygous51465834
105958976759589768TC12GENIChomozygous51465835
105959129359591300GGCATTT-------7GENIChomozygous51465836
105959390759593908TC21GENICpossibly homozygous51465837
105959710559597106GGC8GENICheterozygous51465838
105959928459599285GT24GENICpossibly homozygous51465839
105960012859600129G-9GENIChomozygous51465841
105960650559606506CT20GENICpossibly homozygous51465846