chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154280894542808946TC33GENIChomozygous112494720
154280937442809375TG49GENIChomozygous112673631
154280991342809914AC39GENICpossibly homozygous112494722
154280999842809999CT43GENIChomozygous112494724
154281056642810567CT32GENIChomozygous112673633
154281081942810820TG46GENIChomozygous112494728
154281155242811553TC25GENIChomozygous112494730
154281300742813008AG43GENIChomozygous112494732
154281356242813563GA23GENIChomozygous112673635
154281622842816229TC29GENIChomozygous112673637
154281644942816450CT47GENIChomozygous112673639
154281745142817452CG34GENIChomozygous112673641
154281819642818197CT31GENIChomozygous112494734
154281848742818488AG34GENIChomozygous112494736
154282046742820468GA47GENIChomozygous112673643
154282119442821195GA33GENICpossibly homozygous112494738
154282134042821341CG28GENIChomozygous112494740
154282141542821416CG36GENICpossibly homozygous112673645
154282231742822318AT44GENIChomozygous112673647
154282255342822554TC31GENIChomozygous112494744
154282267242822673TC46GENIChomozygous112494746
154282332242823323CT26GENIChomozygous112673649
154282396742823968AT42GENICpossibly homozygous112673651
154282450442824505GT47GENICpossibly homozygous112673653
154282470542824706TC30GENIChomozygous112494750
154282517242825173CT35GENIChomozygous112673655