chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56212919862129199TC26GENIChomozygous113830720
56212958762129588CA27GENIChomozygous113830722
56212964662129647CT41GENIChomozygous113830726
56212985762129858GA30GENIChomozygous113830728
56213014862130149GC36GENIChomozygous113830730
56213016062130161GA36GENIChomozygous113830732
56213105662131057GA39GENIChomozygous113830734
56213216162132162AG27GENIChomozygous113830736
56213233862132339GA26GENIChomozygous113830738
56213349062133491TC23GENIChomozygous113830746
56213357062133571GT17GENIChomozygous113830748
56213434662134347GA24GENIChomozygous113830752
56213475662134757AG11GENIChomozygous113830754
56213479162134792GA11GENIChomozygous113830756
56213480262134803AG12GENIChomozygous113830758
56213501762135018TG21GENIChomozygous113830762
56213528662135287TC26GENIChomozygous113830764
56213592162135922GA53GENIChomozygous113830766
56213695162136952TG24GENIChomozygous113830768
56213850862138509TC9GENIChomozygous113830778
56213889662138897CG21GENIChomozygous113830780
56213903562139036GA28GENIChomozygous113830782
56214147162141472CT20GENIChomozygous113830784
56214147262141473AG20GENIChomozygous113830786
56214236362142364GA23GENIChomozygous113830788
56214412862144129CT26GENIChomozygous113830798
56214427262144273AC28GENIChomozygous113830800
56214506262145063TC21GENIChomozygous113830802
56214527762145278CT28GENICpossibly homozygous113830804
56214568762145688CT20GENIChomozygous113830806
56214576962145770TC19GENIChomozygous113830808
56214695062146951TC18GENIChomozygous113830810
56215027862150279GA30GENIChomozygous113830820
56215064162150642CT28GENIChomozygous113830822
56215092462150925CT28GENIChomozygous113830824
56215111962151120AC26GENIChomozygous113830826
56215161962151620AG9GENIChomozygous113830828
56215201862152019AG37GENIChomozygous113830830
56215335162153352AG20GENIChomozygous113830832