chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105958711059587111CT15GENICpossibly homozygous51465833
105958767859587679CT18GENICheterozygous51465834
105958976759589768TC9GENIChomozygous51465835
105959129359591300GGCATTT-------10GENICpossibly homozygous51465836
105959390759593908TC29GENICpossibly homozygous51465837
105959710559597106GGC10GENICheterozygous51465838
105959928459599285GT28GENIChomozygous51465839
105960012859600129G-15GENICpossibly homozygous51465841
105960650559606506CT27GENIChomozygous51465846