chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167221658772216588TA18GENICheterozygous119221781
167221672172216722CT37GENICheterozygous119233528
167221700772217008AC19GENIChomozygous111856982
167221764672217647AC34GENIChomozygous111856989
167221775572217756AG30GENIChomozygous112077987
167221889672218897AG23GENIChomozygous112077989
167221918772219188AC35GENIChomozygous112027854
167221923272219233CA29GENIChomozygous112077991
167221938272219383CT18GENIChomozygous112077993
167221959172219592TC27GENIChomozygous111857014
167221960272219603TC27GENICpossibly homozygous112077995
167222015172220152CT41GENIChomozygous112077999
167222050872220509CT21GENIChomozygous112078001
167222283372222834GA20GENIChomozygous112078003
167222321972223220AC23GENICpossibly homozygous111857058
167222367872223679GA12GENIChomozygous112078005
167222397972223980GA15GENIChomozygous112078007
167222445372224454CT29GENIChomozygous111857079
167222501972225020GA28GENIChomozygous111857081
167222683172226832CT22GENIChomozygous112078009
167222712372227124CA29GENIChomozygous112078011
167222735872227359CT18GENIChomozygous112078013
167222787472227875AG30GENIChomozygous112078015
167221751472217515GC27GENIChomozygous112212061