chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216243136216243137TC28GENIChomozygous108535662
1216244210216244211GA44GENIChomozygous108535664
1216244909216244910CT30GENIChomozygous109193052
1216245558216245559CA44GENICpossibly homozygous109193054
1216245648216245649GA39GENICpossibly homozygous109193056
1216245986216245987AG44GENIChomozygous108535665
1216246544216246545CT43GENICpossibly homozygous109193058
1216246631216246632TC39GENIChomozygous108535666
1216246684216246685TC36GENIChomozygous109193060
1216246882216246883AG51GENIChomozygous109193062
1216247223216247224CG48GENIChomozygous109193064
1216247338216247339TC31GENIChomozygous109193066
1216248085216248086AG30GENIChomozygous109193068
1216248270216248271AG37GENIChomozygous109193070
1216248507216248508GA33GENIChomozygous109193072
1216248632216248633TC35GENIChomozygous109193074
1216248649216248650TA33GENIChomozygous109193076
1216249216216249217AG40GENIChomozygous109193078
1216249247216249248AG35GENIChomozygous109193080
1216249448216249449AG25GENIChomozygous109193082
1216249571216249572TC40GENIChomozygous109193084
1216250044216250045GC39GENIChomozygous109193086
1216250107216250108AG36GENIChomozygous109193088
1216250218216250219CT39GENICpossibly homozygous109193090
1216250400216250401AT41GENIChomozygous109193092
1216250444216250445AG32GENIChomozygous108535668
1216250454216250455AC32GENIChomozygous109193094
1216250497216250498CA30GENIChomozygous109193096
1216250955216250956TC28GENICpossibly homozygous109193098
1216251180216251181CA32GENIChomozygous109193100
1216251361216251362TC43GENIChomozygous109193102
1216251420216251421GA40GENIChomozygous109193104
1216251893216251894CT31GENIChomozygous109193106
1216251926216251927TC33GENIChomozygous109193108
1216252757216252758CT35GENIChomozygous109193110
1216252941216252942AG37GENIChomozygous109193112
1216252964216252965GT38GENIChomozygous109193114
1216252983216252984AC35GENICpossibly homozygous109193116