chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144148528541485286GA13GENIChomozygous139523741
144148529741485298GA12GENIChomozygous139523742
144148559741485598AG26GENIChomozygous139523743
144148564241485643GT23GENIChomozygous144129021
144148615641486157AC31GENICpossibly homozygous139523744
144148628941486290AC23GENIChomozygous139523745
144148674641486747GA17GENIChomozygous139523746
144148678341486784CA16GENIChomozygous139523747
144148694341486944CG15GENIChomozygous139523748
144148700941487010AG12GENIChomozygous139523749
144148710141487102GA18GENIChomozygous139523750
144148736641487367CT22GENIChomozygous139523751
144148740141487402AG25GENIChomozygous139523752
144148771541487716CT22GENIChomozygous139523753
144148847741488478GA22GENIChomozygous139523754
144148851641488517AG23GENIChomozygous139523755
144148870241488703TC23GENIChomozygous139523756
144148881941488820GC18GENIChomozygous139523757
144148958841489589CT19GENIChomozygous139523758
144148969241489693GA14GENIChomozygous139523759
144148992141489922GT10GENIChomozygous139523760
144149007441490075TA12GENICpossibly homozygous139523761
144149008441490084CTA12GENIChomozygous139395192
144148788441487886TG30GENIChomozygous139395189
144148861741488617AC19GENICpossibly homozygous139395190
144148864941488649GG24GENIChomozygous139395191
144149069941490700CT20GENIChomozygous139523762
144149078241490783TC23GENIChomozygous139523763
144149089541490895C21GENIChomozygous139395193
144149114141491142GA12GENIChomozygous139523764
144149191841491919C14GENIChomozygous139395194
144149223141492232GA20GENIChomozygous139523765
144149224341492244TC20GENIChomozygous139523766
144149346441493464C9GENICheterozygous139395195
144149375841493759TG17GENIChomozygous139523768
144149432141494321G12GENIChomozygous139395196
144149219741492198A13GENICheterozygous403654427
144149219741492198AT13GENICheterozygous154855815
144149290541492906C10GENIChomozygous403358552
144149290541492906CG10GENICheterozygous403358553
144149521441495215AG10GENIChomozygous139523769