chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144148528541485286GA16GENIChomozygous139523741
144148529741485298GA21GENIChomozygous139523742
144148559741485598AG16GENIChomozygous139523743
144148564241485643GT16GENIChomozygous144129021
144148615641486157AC24GENIChomozygous139523744
144148628941486290AC25GENIChomozygous139523745
144148674641486747GA22GENIChomozygous139523746
144148678341486784CA24GENIChomozygous139523747
144148694341486944CG13GENIChomozygous139523748
144148700941487010AG9GENIChomozygous139523749
144148710141487102GA17GENIChomozygous139523750
144148736641487367CT22GENIChomozygous139523751
144148740141487402AG18GENIChomozygous139523752
144148771541487716CT24GENIChomozygous139523753
144148847741488478GA20GENIChomozygous139523754
144148851641488517AG19GENIChomozygous139523755
144148870241488703TC16GENIChomozygous139523756
144148881941488820GC20GENIChomozygous139523757
144148958841489589CT22GENIChomozygous139523758
144148969241489693GA18GENIChomozygous139523759
144148992141489922GT12GENIChomozygous139523760
144149007441490075TA14GENIChomozygous139523761
144149008441490084CTA15GENIChomozygous139395192
144148788441487886TG11GENIChomozygous139395189
144148861741488617AC16GENIChomozygous139395190
144148864941488649GG13GENIChomozygous139395191
144149069941490700CT20GENIChomozygous139523762
144149078241490783TC26GENIChomozygous139523763
144149089541490895C16GENIChomozygous139395193
144149114141491142GA18GENIChomozygous139523764
144149191841491919C10GENIChomozygous139395194
144149223141492232GA12GENIChomozygous139523765
144149224341492244TC14GENIChomozygous139523766
144149346441493464C13GENIChomozygous139395195
144149375841493759TG8GENIChomozygous139523768
144149432141494321G17GENICpossibly homozygous139395196
144149521441495215AG16GENIChomozygous139523769
144149290541492906CG21GENICheterozygous403358553
144149219741492198AT12GENICheterozygous154855815
144149219741492198A12GENIChomozygous403654427
144149290541492906C21GENIChomozygous403358552