chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230472827230472828CT22GENIChomozygous59431943
2230473512230473513CT33GENICpossibly homozygous59431944
2230473813230473814CT29GENIChomozygous59431945
2230473897230473898AG33GENICpossibly homozygous59431946
2230473898230473899CG34GENICpossibly homozygous59431947
2230474730230474731GA28GENIChomozygous59431949
2230475825230475826GA23GENIChomozygous59431951
2230476295230476296T-10GENIChomozygous59431952
2230476539230476540CCCA2GENIChomozygous60520653
2230477143230477144CT35GENICpossibly homozygous59431953
2230477381230477382GA30GENICpossibly homozygous59431954
2230477500230477501TC32GENIChomozygous59431955
2230477896230477897AAG31GENICpossibly homozygous59431956
2230478593230478594AG34GENIChomozygous59431957
2230479347230479348AG14GENICpossibly homozygous59431959
2230479988230479989AT23GENIChomozygous59431961
2230480119230480120GC16GENIChomozygous59431962
2230480287230480288TC29GENIChomozygous59431963
2230480429230480430TC33GENIChomozygous59431964
2230480682230480683TC29GENICpossibly homozygous59431965
2230480871230480872AC30GENICpossibly homozygous59431966
2230481238230481239CT11GENIChomozygous59431967
2230482198230482199TC29GENIChomozygous59431968
2230482668230482669AG27GENICpossibly homozygous59431969
2230482731230482732CCTTCATTCA16GENIChomozygous59431970
2230483192230483193AG35GENIChomozygous59431971
2230483236230483237TC41GENIChomozygous59431972
2230483327230483328CT28GENIChomozygous59431973
2230483472230483473GA37GENIChomozygous59431974
2230483797230483798GA26GENIChomozygous59431975
2230484491230484492CT28GENIChomozygous59431976
2230484580230484581GA23GENIChomozygous59431977
2230484922230484923TC21GENIChomozygous59431978
2230486073230486077TTCA----21GENIChomozygous59431979
2230486117230486118TC25GENIChomozygous59431981