chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
731451253145126AG12GENIChomozygous115977573
731456263145627GC14GENIChomozygous115546715
731461523146153TC15GENIChomozygous115546719
731464903146491GA16GENIChomozygous115977575
731465343146535T15GENIChomozygous133486165
731477573147757C10GENIChomozygous133486166
731479883147989CT11GENIChomozygous115977577
731486203148621CG8GENIChomozygous115977579
731487043148705AG17GENIChomozygous115977581
731487423148743CT17GENIChomozygous115977583
731488403148841CG11GENIChomozygous115977585
731488963148897GA17GENIChomozygous115546727
731490313149032AC11GENIChomozygous115977587
731495083149509GC8GENIChomozygous115977589
731504123150413AT20GENIChomozygous115977591
731504973150497A6GENIChomozygous131007073
731505063150507GA7GENIChomozygous116268582
731516003151601CT6GENIChomozygous116401262
731516023151603CT6GENIChomozygous133487558
731524333152434GT13GENIChomozygous115977593
731526573152667GCCTGCCTCT19GENIChomozygous133486167
731529163152917A18GENIChomozygous131007075
731529703152970TG16GENIChomozygous131007076
731537083153728CGCGTGTGCACGTGCACAGA13GENIChomozygous133486168
731543393154340A13GENIChomozygous131007077
731554633155464GA14GENIChomozygous115977595
731555043155504CACAGGGAGATCCCTGGGCT18GENIChomozygous128432470
731560083156009CG17GENIChomozygous115546739
731569653156966AG9GENIChomozygous115977597
731585863158586GG8GENIChomozygous133486170
731642053164206CT9GENIChomozygous115546745
731642353164235T11GENICpossibly homozygous131007079
731653203165321CG13GENIChomozygous115977599
731680303168031TC18GENIChomozygous115546753
731693223169322CGGAGGGTGT19GENIChomozygous128432475
731696633169664GT15GENIChomozygous115977601
731520843152084T13GENICpossibly homozygous130560648