chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161869292318692924GT22GENIChomozygous111749515
161869292418692925TA22GENIChomozygous111749517
161869293518692936GT20GENIChomozygous111749519
161869297118692972GA14GENIChomozygous111749527
161869299018692991AG14GENIChomozygous111749531
161869299718692998CT14GENIChomozygous111749533
161869300418693005CT13GENIChomozygous111749535
161869300518693006TC13GENIChomozygous111749537
161870043518700436TC11GENIChomozygous111749541
161870089718700898GA17GENIChomozygous111945388
161870259918702600TC20GENIChomozygous111749547
161870334718703348AG14GENIChomozygous111749549
161870363718703638AG22GENIChomozygous111749551
161870441718704418CT21GENIChomozygous111749553
161870676118706762TC37GENIChomozygous111749559
161870757518707576TC29GENIChomozygous111749565
161870761218707613TA27GENIChomozygous111749567
161870773218707733AG15GENIChomozygous111749570
161870779918707800CT27GENIChomozygous111749572
161870802718708028GA25GENIChomozygous112150129
161870501818705019GA38GENIChomozygous112150123
161870770118707702GA19GENIChomozygous112150127
161870672218706723CT31GENIChomozygous112291474
161870815518708156TC20GENIChomozygous111749574
161870864218708643AG28GENIChomozygous111749576
161870880918708810CG27GENIChomozygous111749578
161870904318709044CT23GENIChomozygous111749580
161870906518709066AG20GENIChomozygous111749582