chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56212919862129199TC21GENIChomozygous113830720
56212958762129588CA23GENIChomozygous113830722
56212964462129645CT29GENIChomozygous113830724
56212964662129647CT28GENIChomozygous113830726
56212985762129858GA28GENIChomozygous113830728
56213014862130149GC19GENIChomozygous113830730
56213016062130161GA22GENIChomozygous113830732
56213105662131057GA29GENIChomozygous113830734
56213216162132162AG15GENIChomozygous113830736
56213233862132339GA25GENIChomozygous113830738
56213349062133491TC13GENIChomozygous113830746
56213357062133571GT7GENIChomozygous113830748
56213434662134347GA24GENIChomozygous113830752
56213475662134757AG8GENIChomozygous113830754
56213501762135018TG9GENIChomozygous113830762
56213528662135287TC18GENIChomozygous113830764
56213592162135922GA35GENIChomozygous113830766
56213695162136952TG19GENIChomozygous113830768
56213850862138509TC6GENIChomozygous113830778
56213889662138897CG23GENIChomozygous113830780
56213903562139036GA13GENIChomozygous113830782
56214147162141472CT16GENIChomozygous113830784
56214147262141473AG15GENIChomozygous113830786
56214236362142364GA17GENIChomozygous113830788
56214295662142957CT36GENICheterozygous113830794
56214412862144129CT19GENIChomozygous113830798
56214427262144273AC29GENIChomozygous113830800
56214506262145063TC19GENIChomozygous113830802
56214527762145278CT22GENIChomozygous113830804
56214568762145688CT13GENIChomozygous113830806
56214576962145770TC7GENIChomozygous113830808
56214695062146951TC15GENIChomozygous113830810
56215027862150279GA25GENICpossibly homozygous113830820
56215064162150642CT20GENIChomozygous113830822
56215092462150925CT26GENIChomozygous113830824
56215201862152019AG21GENIChomozygous113830830
56215335162153352AG9GENIChomozygous113830832
56215360862153609AG6GENIChomozygous113830834