chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18500366485003665CG18GENIChomozygous109504192
18500676385006764CT28GENIChomozygous108881548
18500679785006798GA29GENIChomozygous108881550
18500656985006570CT26GENIChomozygous108881547
18500679685006797TC29GENIChomozygous108881549
18500694485006945GT33GENIChomozygous108881551
18500698585006986AG35GENIChomozygous108881552
18500703185007032GA25GENIChomozygous108881553
18500720085007201GA19GENIChomozygous108881554
18500541685005417TG43GENIChomozygous120482898
18500741285007413GA28GENIChomozygous120482899
18501352585013526GA18GENIChomozygous120482901
18501359385013594CT28GENIChomozygous120482902
18501861785018618CT34GENIChomozygous120482903
18501911485019115CT28GENIChomozygous109504249
18501990785019908TA32GENIChomozygous120482904
18502063185020632GA30GENIChomozygous120482905
18502103585021036AG24GENIChomozygous120482906
18502107685021077CA30GENIChomozygous120482907
18502194285021943AG19GENIChomozygous109504251
18502460085024601CT25GENIChomozygous108881561
18502465485024655GA26GENIChomozygous108881562
18502479885024799GA32GENIChomozygous120482908
18502548885025489GA23GENIChomozygous108881563
18502594285025943AT25GENIChomozygous120482909
18502673285026733TC19GENIChomozygous108881564
18502741485027415TC20GENIChomozygous108881565
18502824385028244CA24GENIChomozygous108881567
18502896685028967GA23GENIChomozygous108881569
18502898985028990GT19GENICpossibly homozygous120482910
18502947285029473AG18GENIChomozygous109504267
18503019885030199CA36GENIChomozygous109504268
18503373785033738AG17GENIChomozygous108881576
18502633785026338CT8GENIChomozygous109109228
18503055085030551TC28GENIChomozygous108881572
18503415385034154GT26GENIChomozygous120482911
18503799285037993CT27GENIChomozygous120482912
18504158385041584GA37GENIChomozygous108881590
18504275385042754TG36GENIChomozygous108881591