chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161869139718691398GA22GENIChomozygous111749511
161869195418691955CT25GENIChomozygous111749513
161869298118692982GT14GENIChomozygous111749529
161869302018693021CG7GENIChomozygous125653903
161869418518694186GA23GENIChomozygous111749539
161870043518700436TC21GENIChomozygous111749541
161870107218701073GA20GENIChomozygous111749543
161870163818701639CG13GENIChomozygous111749545
161870259918702600TC7GENIChomozygous111749547
161870334718703348AG10GENIChomozygous111749549
161870363718703638AG15GENICheterozygous111749551
161870441718704418CT5GENIChomozygous111749553
161870476118704762CT12GENIChomozygous111749555
161870532118705322TC12GENIChomozygous111749557
161870676118706762TC21GENIChomozygous111749559
161870690018706901GA19GENIChomozygous111749561
161870696718706968CT20GENIChomozygous111749563
161870757518707576TC21GENIChomozygous111749565
161870761218707613TA20GENIChomozygous111749567
161870773218707733AG18GENIChomozygous111749570
161870779918707800CT19GENIChomozygous111749572
161870815518708156TC24GENIChomozygous111749574
161870864218708643AG14GENIChomozygous111749576
161870880918708810CG16GENIChomozygous111749578
161870904318709044CT18GENIChomozygous111749580
161870906518709066AG25GENIChomozygous111749582