chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124069586340695864CT16GENIChomozygous958965871
124069615140696152GA30GENIChomozygous958965872
124069621640696217TC27GENIChomozygous958965873
124069664840696649AT15GENIChomozygous958965874
124069688440696885AT13GENIChomozygous958965875
124069702040697021AC15GENICpossibly homozygous958965876
124069744640697447TC19GENIChomozygous958965877
124069746740697468CT24GENIChomozygous958965878
124069828240698283CA20GENIChomozygous958965879
124069893540698936AG22GENIChomozygous958965880
124070058640700587TC13GENIChomozygous958965881
124070295940702960TC36GENIChomozygous958965882
124070382840703829CA31GENIChomozygous958965883
124070532540705326AG19GENIChomozygous958965884
124070747640707477CT29GENIChomozygous958965885