chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832057478320575AG17GENIChomozygous886013774
47832062078320621AC11GENIChomozygous886013775
47832063878320639CA12GENIChomozygous886013776
47832081578320816GA21GENIChomozygous886013777
47832140078321401TC18GENIChomozygous886013778
47832144778321448TA23GENIChomozygous886013779
47832274678322747CA12GENIChomozygous886013780
47832291378322914TA13GENIChomozygous886013781
47832291878322919CA14GENIChomozygous886013782
47832306478323065CT12GENIChomozygous886013783
47832315378323154GA21GENIChomozygous886013784
47832367778323678GA27GENIChomozygous886013785
47832382878323829TC6GENIChomozygous886013786
47832399678323997GA14GENIChomozygous886013787
47832419778324198CT17GENIChomozygous886013788
47832429778324298CT12GENIChomozygous886013789
47832433978324340GT6GENIChomozygous886013790
47832469278324693TA19GENIChomozygous886013791
47832473778324738GC23GENIChomozygous886013792
47832505378325054AG22GENIChomozygous886013793
47832524978325250CT22GENIChomozygous886013794
47832595578325956AG22GENIChomozygous886013795
47832653078326531AG28GENIChomozygous886013796
47832659078326591AG27GENIChomozygous886013797
47832682978326830TC22GENIChomozygous886013798
47832691478326915AG18GENIChomozygous886013799
47832703778327038TC8GENIChomozygous886013800