chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167067948470679485CT12GENIChomozygous47788116
167068083570680836AG11GENICpossibly homozygous47788117
167068179870681799AC14GENIChomozygous47788118
167068314170683142CCTG6GENIChomozygous47691768
167068605170686052CT10GENIChomozygous47788120
167068605570686056CT11GENIChomozygous47788121
167069110970691110TA9GENIChomozygous47788123
167069354970693550GC18GENIChomozygous47788124
167069378970693790AG14GENIChomozygous47691777
167069453270694533CT21GENICpossibly homozygous47691778
167069634670696347TC5GENIChomozygous47691779