chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG23GENIChomozygous945996006
1266867306266867307GA37GENIChomozygous945996007
1266868276266868277AT13GENIChomozygous945996008
1266868839266868840GA30GENIChomozygous945996009
1266869162266869163TC24GENIChomozygous945996010
1266869171266869172TC23GENIChomozygous945996011
1266869515266869516AG22GENIChomozygous945996012
1266870524266870525AG18GENIChomozygous945996013
1266870982266870983GC18GENIChomozygous945996014
1266871531266871532AG25GENIChomozygous945996015
1266871799266871800AG26GENIChomozygous945996016
1266876378266876379AG20GENIChomozygous945996017
1266876812266876813GA24GENIChomozygous945996018
1266877785266877786CT29GENIChomozygous945996019
1266879795266879796TG33GENIChomozygous945996020
1266881721266881722AG25GENIChomozygous945996021
1266882385266882386GC27GENIChomozygous945996022
1266884148266884149CG29GENIChomozygous945996023
1266885292266885293AC32GENIChomozygous945996024
1266885604266885605GA25GENIChomozygous945996025
1266887077266887078GA14GENIChomozygous945996026
1266888529266888530CT11GENIChomozygous945996027
1266889651266889652TC33GENIChomozygous945996028
1266890046266890047TC25GENIChomozygous945996029
1266890845266890846GA23GENIChomozygous945996030
1266892448266892449AG23GENICpossibly homozygous945996031
1266892512266892513TC28GENIChomozygous945996032
1266894775266894776GA31GENIChomozygous945996033
1266895476266895477AG32GENIChomozygous945996034
1266897388266897389TC23GENIChomozygous945996035
1266897444266897445CT21GENIChomozygous945996036
1266897506266897507GA11GENIChomozygous945996037
1266899513266899514GA11GENIChomozygous945996038
1266906928266906929AC19GENIChomozygous945996039
1266907705266907706AT20GENIChomozygous945996040
1266907761266907762CG20GENIChomozygous945996041
1266907786266907787GA25GENIChomozygous945996042