chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486261224862613GA11GENIChomozygous650759559
162486311324863114CCGT9GENICpossibly homozygous757548652
162486320324863204TA15GENIChomozygous650759560
162486389124863892GC26GENIChomozygous650759561
162486527524865276A-24GENIChomozygous757548653
162486529824865299AG27GENIChomozygous650759562
162486561624865617CT23GENIChomozygous650759563
162486564024865664TCTTTCTTTCTTTCTTTCTTTCTT------------------------4GENIChomozygous757548654
162486585924865860TG15GENIChomozygous650759564
162486707024867071T-18GENIChomozygous757548657
162486855024868551CT23GENIChomozygous650759565
162486940724869408TA26GENIChomozygous650759566
162486959324869594CT16GENIChomozygous650759567
162486974824869749AT14GENIChomozygous650759568
162487061224870613AG17GENIChomozygous650759569
162487061424870615TC16GENIChomozygous650759570
162487064724870648GA16GENIChomozygous650759571
162487067424870675CT14GENIChomozygous650759572
162487135524871356CG22GENIChomozygous650759573
162487138324871384A-6GENICheterozygous757548658