chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108158936181589362AG37GENIChomozygous116811867
108158944381589444AG29GENIChomozygous116811869
108159202381592024CG33GENIChomozygous116811871
108159204981592050TC40GENIChomozygous116811873
108160057581600576AG25GENIChomozygous116811875
108160186881601869TC18GENIChomozygous116811877
108160232181602322GA25GENIChomozygous116811879
108160424481604245AC26GENIChomozygous116811881
108160485681604857GA33GENIChomozygous116811883
108160568281605683GT32GENICpossibly homozygous116811885
108160747781607478AG30GENIChomozygous116811887
108160859681608597GA19GENIChomozygous116811889
108161649681616497GT33GENIChomozygous116811891
108161816281618163GA25GENIChomozygous116811893
108161951481619515TA29GENIChomozygous116657279
108162159681621597GA16GENIChomozygous116811895
108162225281622253GA25GENIChomozygous116811897
108162323481623235CT26GENIChomozygous116811899
108162494281624943GA18GENIChomozygous116811901
108162719781627198AG34GENIChomozygous116657285
108163106781631068TA9GENIChomozygous116657287
108163214981632150TG24GENIChomozygous116811903
108163307381633074TC24GENIChomozygous116657289
108164050881640509CT31GENIChomozygous116657296
108163332481633325GT19GENIChomozygous116811905
108163344581633446AG26GENIChomozygous116811907
108163859081638591TC22GENICpossibly homozygous116811909
108163886281638863GT37GENIChomozygous116811911
108162660781626608AG7GENIChomozygous117133497
108164179481641795TG33GENIChomozygous116657298
108164198481641985TA33GENIChomozygous116811917
108164373781643738CT22GENIChomozygous116811919