chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763983717639838GC19GENIChomozygous890577806
141763993717639938GA22GENIChomozygous890577807
141763996417639965AG23GENIChomozygous890577808
141764000017640001CT20GENIChomozygous890577809
141764015017640151CG14GENIChomozygous890577810
141764052717640528GT12GENIChomozygous890577811
141764053317640534GA14GENICheterozygous890577812
141764171317641714CT6GENIChomozygous890577813
141764232617642327AT9GENICheterozygous890577814
141764266917642670AG18GENIChomozygous890577815
141764287317642874GT13GENIChomozygous890577816
141764307417643075CT21GENIChomozygous890577817
141764414917644150CA21GENIChomozygous890577818
141764869017648691GC7GENIChomozygous890577819
141765011617650117CA13GENIChomozygous890577820
141765030017650301TC8GENIChomozygous890577821
141765031617650317TC15GENIChomozygous890577822
141765040117650402TC11GENIChomozygous890577823
141765048617650487CT7GENIChomozygous890577824
141765056917650570CT5GENIChomozygous890577825
141765061417650615CT19GENIChomozygous890577826
141765067217650673TG7GENIChomozygous890577827
141765072117650722AG6GENIChomozygous890577828
141765073017650731CT7GENIChomozygous890577829
141765112317651124TA13GENIChomozygous890577830
141765115717651158AT8GENIChomozygous890577831
141765116317651164GA9GENIChomozygous890577832
141765141217651413AT19GENIChomozygous890577833
141765144717651448TG23GENIChomozygous890577834
141765161617651617AG12GENIChomozygous890577835
141765171117651712GC5GENIChomozygous890577836
141765171817651719GA4GENIChomozygous890577837
141765172617651727GT5GENIChomozygous890577838
141765179617651797GA6GENIChomozygous890577839
141765377317653774AG13GENIChomozygous890577840
141765381117653812AG10GENIChomozygous890577841
141765416217654163AG5GENIChomozygous890577842
141765438217654383CA10GENIChomozygous890577843
141765581617655817TC31GENIChomozygous890577844
141765617717656178TG13GENIChomozygous890577845
141765645617656457TC20GENIChomozygous890577846
141765685017656851AG21GENIChomozygous890577847