chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57637673676376737AC4GENIChomozygous118942702
57637673676376736G4GENIChomozygous128200000
57637674976376750GC3GENIChomozygous113870553
57637692076376920A5GENIChomozygous129914844
57637679976376800G1GENIChomozygous129914841
57637690976376909C5GENIChomozygous129914843
57637694676376946G10GENIChomozygous129914845
57637697476376975C10GENIChomozygous129914846
57637701376377013G8GENIChomozygous129914847
57637702676377027C7GENIChomozygous129914848
57638723076387231T5GENIChomozygous128200001
57638994876389949TG8GENIChomozygous126196434
57639216776392168GA22GENIChomozygous113870555
57639267476392675GA20GENIChomozygous113870557
57639287276392873GA24GENIChomozygous113870559
57639496676394967CT18GENIChomozygous113870561
57639738276397383CG16GENIChomozygous113870563
57639753176397532GA23GENIChomozygous113870565
57637702176377022AG8GENIChomozygous114126605
57640109976401100CT13GENIChomozygous113870567
57640126276401264TC10GENIChomozygous128200003
57640495376404954CT24GENIChomozygous113870569
57640539176405392CT20GENIChomozygous113870571
57640582776405831TTTG16GENIChomozygous128200004
57641207876412079AG22GENIChomozygous113870573
57641221276412213CT21GENIChomozygous113870575
57641570576415706CT17GENIChomozygous113870577
57641587376415874AG16GENIChomozygous113870579
57641597176415971GTGTGA7GENIChomozygous128200005
57641598576415986GT5GENIChomozygous113870581
57641647676416477GA14GENICheterozygous113870591
57641728776417289AT4GENIChomozygous128200007
57641752276417523GT13GENIChomozygous113870597
57641925876419258A13GENICheterozygous129914852
57640448876404489TC23GENICpossibly homozygous128289566