chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486261224862613GA34GENIChomozygous522246025
162486311324863114CCGT28GENICpossibly homozygous691462942
162486320324863204TA37GENIChomozygous521133118
162486389124863892GC34GENIChomozygous521133119
162486527524865276A-26GENIChomozygous691462943
162486529824865299AG32GENIChomozygous521133120
162486561624865617CT42GENICpossibly homozygous521133121
162486567224865673TC25GENICheterozygous521133122
162486568424865685TC26GENICheterozygous521133123
162486585924865860TG31GENIChomozygous521133124
162486707024867071T-36GENIChomozygous691462944
162486855024868551CT42GENIChomozygous521133125
162486940724869408TA48GENIChomozygous521133126
162486959324869594CT37GENIChomozygous521133127
162487061224870613AG37GENIChomozygous521133128
162487061424870615TC35GENIChomozygous521133129
162487064724870648GA29GENIChomozygous521133130
162487067424870675CT29GENIChomozygous521133131
162487135524871356CG45GENICpossibly homozygous521133132
162487162424871625TG32GENICheterozygous522246026