chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105958711059587111CT15GENIChomozygous51465833
105958767859587679CT13GENICheterozygous51465834
105959307559593076CA12GENICheterozygous51663685
105959390759593908TC12GENIChomozygous51465837
105959579159595792CT7GENICheterozygous51663687
105959710559597106GGC5GENICheterozygous51465838
105959928459599285GT25GENICpossibly homozygous51465839
105960012859600129G-5GENIChomozygous51465841
105960068259600683GGTT2GENIChomozygous51465843
105960463559604636T-3GENICheterozygous51465844
105960650559606506CT14GENIChomozygous51465846