chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
24326841243268413AG18GENIChomozygous120166877
24326962743269628CT13GENIChomozygous120166878
24326970843269709TG10GENIChomozygous109721042
24327027343270274TC6GENIChomozygous120166879
24327138043271381TC18GENIChomozygous120166880
24327229943272300AG28GENIChomozygous120166881
24327261243272613AG16GENIChomozygous120166882
24327402343274024TC19GENIChomozygous120166884
24327469143274692AT19GENIChomozygous109721050
24327542343275424CA13GENIChomozygous120166885
24327552243275523CT15GENIChomozygous120166886
24327558743275588GT12GENIChomozygous120166887
24327588643275887TA12GENIChomozygous120166888
24327603443276035AG21GENIChomozygous120166889
24327785743277858TC16GENIChomozygous109721058
24327811043278111CT10GENICheterozygous120166890
24327821543278216AG19GENIChomozygous120166891
24327983343279834TC20GENIChomozygous109721072
24328056343280564GC14GENIChomozygous109721074
24328131843281319CT25GENIChomozygous109721076
24328172243281723TA15GENIChomozygous120166892
24328181743281818AG16GENIChomozygous109721078
24328232243282323TG20GENIChomozygous109721082
24328340943283410GA16GENIChomozygous109721084
24328428443284285CG8GENIChomozygous120166893
24328444743284448TC14GENIChomozygous109721090
24328465943284660AG14GENIChomozygous109721092
24328478443284785TC12GENICheterozygous109721094
24328641543286416GT7GENIChomozygous111240027
24328648343286484CT11GENIChomozygous109721118
24328697143286972CT11GENIChomozygous109721126
24328709043287091AG16GENIChomozygous109721128
24328871643288717AG17GENIChomozygous109721138
24328877543288776GT16GENIChomozygous109721140
24328882843288829GA15GENIChomozygous111240029
24328934443289345TG21GENIChomozygous109721146
24328612943286130CT19GENIChomozygous125639738