chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671435066714351GA20GENIChomozygous874720826
116671589766715898GA28GENIChomozygous874720827
116671647966716480TC19GENIChomozygous874720828
116671668466716685GA10GENIChomozygous874720829
116671751166717512CG4GENIChomozygous874720830
116671755366717554CA16GENIChomozygous874720831
116671760366717604GC23GENIChomozygous874720832
116671894366718944AG18GENIChomozygous874720833
116672098466720985TA6GENIChomozygous874720834
116672164466721645TC18GENIChomozygous874720835
116672230266722303GA20GENIChomozygous874720836
116672248866722489TG17GENIChomozygous874720837
116672292266722923GT15GENIChomozygous874720838
116672350966723510TC18GENIChomozygous874720839
116672355566723556CT19GENIChomozygous874720840
116672411266724113AC23GENIChomozygous874720841
116672493366724934CG15GENIChomozygous874720842
116672502566725026CT24GENIChomozygous874720843
116672543466725435TC29GENIChomozygous874720844
116672601466726015TG14GENIChomozygous874720845
116672636166726362TC9GENIChomozygous874720846
116672647966726480GA21GENIChomozygous874720847
116672675466726755GC24GENIChomozygous874720848
116672734666727347AG16GENIChomozygous874720849
116672929066729291CT13GENIChomozygous874720850
116673084166730842GA9GENIChomozygous874720851
116673086366730864CT16GENIChomozygous874720852