chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486261224862613GA12GENIChomozygous580335898
162486311324863114CCGT6GENIChomozygous717202242
162486320324863204TA8GENICheterozygous579436450
162486389124863892GC14GENIChomozygous579436451
162486527524865276A-19GENIChomozygous717202243
162486529824865299AG17GENIChomozygous579436452
162486561624865617CT1GENIChomozygous579436453
162486585924865860TG21GENICpossibly homozygous579436454
162486707024867071T-12GENICheterozygous717202244
162486855024868551CT12GENIChomozygous579436455
162486940724869408TA22GENICpossibly homozygous579436456
162486959324869594CT21GENICpossibly homozygous579436457
162486974824869749AT15GENIChomozygous579436458
162487061224870613AG14GENIChomozygous579436459
162487061424870615TC12GENIChomozygous579436460
162487064724870648GA15GENICpossibly homozygous579436461
162487067424870675CT19GENIChomozygous579436462
162487135524871356CG8GENICpossibly homozygous579436463