chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85110543051105431CT24GENIChomozygous53116960
85110575551105756AT13GENIChomozygous53116961
85110579251105793TC13GENIChomozygous53116962
85110607951106080CT18GENIChomozygous53116963
85110642151106422AG29GENIChomozygous53116964
85110649551106496AG27GENIChomozygous53116965
85110659351106594AG23GENIChomozygous53116966
85110672751106728CCAG9GENICheterozygous53116968
85110672951106730GGAC11GENICheterozygous53116969
85110673551106736CCAG5GENICheterozygous52972668
85110673751106738GGAC9GENICheterozygous52972669
85110674151106742GC13GENICheterozygous52972670
85110678051106782AG--10GENICheterozygous53181895
85110680151106802G-12GENICheterozygous53116970
85110680351106806GAG---12GENICheterozygous53116971
85110697251106973GA21GENIChomozygous53116972
85110727251107273CT27GENIChomozygous53116973
85110781951107820CG20GENIChomozygous53116974
85110782251107823T-19GENICheterozygous53116975
85110782751107828AT22GENIChomozygous53116976
85110783051107831AAT22GENIChomozygous53116977
85110784351107844CT28GENIChomozygous53116978
85110817151108172AG34GENIChomozygous53116979
85110840751108408GA31GENIChomozygous53116980
85110872651108728TG--14GENIChomozygous53116981
85110902351109024AC28GENIChomozygous53116982
85110906651109067AG26GENIChomozygous53116983
85110928651109287GA15GENIChomozygous53116984
85110955151109552GT22GENIChomozygous53116985
85111014551110146CT34GENIChomozygous53116986
85111036551110366TC28GENIChomozygous53116987
85111148651111487TC24GENIChomozygous53116988
85111172751111728TTG18GENIChomozygous53116989
85111204651112047GA22GENIChomozygous53116990
85111330751113308GC27GENIChomozygous53116991
85111342651113427AT11GENICheterozygous53116992
85111342851113429AT12GENICheterozygous53116993
85110885251108853CG17GENIChomozygous52626232