chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167067737970677380GGGTGTGTGTGTGT8GENIChomozygous47997458
167067948470679485CT21GENIChomozygous47788116
167068083570680836AG23GENIChomozygous47788117
167068179870681799AC12GENIChomozygous47788118
167068314170683142CCTG13GENIChomozygous47691768
167068420770684208GGAGAAAAAGA9GENIChomozygous47788119
167068605170686052CT21GENIChomozygous47788120
167068605570686056CT21GENIChomozygous47788121
167068729870687299GA16GENIChomozygous47788122
167069110970691110TA18GENIChomozygous47788123
167069222470692226TG--12GENICpossibly homozygous47511592
167069306370693064T-10GENIChomozygous47820706
167069354970693550GC25GENIChomozygous47788124
167069378970693790AG22GENIChomozygous47691777
167069453270694533CT23GENIChomozygous47691778
167069607670696090ACACACACACACAC--------------6GENICheterozygous47997459
167069634670696347TC26GENIChomozygous47691779
167069754270697543GGCAGGACAGGACAGGACAGGACAGGA11GENIChomozygous47997460