chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486261224862613GA26GENIChomozygous654558274
162486311324863114CCGT19GENICpossibly homozygous759786422
162486320324863204TA21GENIChomozygous654558275
162486389124863892GC25GENIChomozygous654558276
162486527524865276A-29GENIChomozygous759786423
162486529824865299AG30GENIChomozygous654558277
162486561624865617CT26GENIChomozygous654558278
162486564024865664TCTTTCTTTCTTTCTTTCTTTCTT------------------------14GENIChomozygous759786424
162486585924865860TG41GENIChomozygous654558279
162486707024867071T-27GENIChomozygous759786427
162486855024868551CT37GENIChomozygous654558280
162486940724869408TA34GENIChomozygous654558281
162486959324869594CT20GENIChomozygous654558282
162486974824869749AT23GENIChomozygous654558283
162487061224870613AG25GENIChomozygous654558284
162487061424870615TC24GENIChomozygous654558285
162487064724870648GA25GENIChomozygous654558286
162487067424870675CT29GENIChomozygous654558287
162487135524871356CG16GENIChomozygous654558288
162487138324871384A-10GENICheterozygous759786428