chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167067737970677380GGGTGT5GENIChomozygous47691767
167067948470679485CT42GENIChomozygous47788116
167068083570680836AG28GENIChomozygous47788117
167068179870681799AC30GENIChomozygous47788118
167068314170683142CCTG35GENIChomozygous47691768
167068420770684208GGAGAAAAAGA19GENIChomozygous47788119
167068605170686052CT36GENICpossibly homozygous47788120
167068605570686056CT36GENICpossibly homozygous47788121
167068729870687299GA43GENIChomozygous47788122
167069110970691110TA38GENIChomozygous47788123
167069222470692226TG--37GENICheterozygous47511592
167069354970693550GC33GENIChomozygous47788124
167069378970693790AG37GENIChomozygous47691777
167069453270694533CT41GENIChomozygous47691778
167069634670696347TC48GENIChomozygous47691779
167069754270697543GGCAGGACAGGA5GENIChomozygous47691780
167069306370693064T-1GENIChomozygous47820706
167069222270692226TGTG----37GENICpossibly homozygous47820705