chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117127199117127200GC28GENIChomozygous116670984
8117130615117130616GA27GENIChomozygous116670986
8117132828117132829AC31GENIChomozygous116670988
8117133075117133076CT27GENIChomozygous116670990
8117133443117133444TC29GENIChomozygous116670992
8117134088117134089CT26GENIChomozygous116670994
8117134631117134632CT26GENIChomozygous116670996
8117134718117134719TC27GENIChomozygous116670998
8117135229117135230CT25GENIChomozygous116671000
8117138817117138818CT20GENIChomozygous116671006
8117139505117139506TA21GENIChomozygous116671008
8117140818117140819GA30GENIChomozygous116671012
8117144080117144081AG29GENIChomozygous116671016
8117148691117148692CT31GENIChomozygous116671024
8117149567117149568TA22GENIChomozygous116671026
8117150952117150953GA28GENIChomozygous116671028
8117153648117153649AT31GENIChomozygous116671034
8117154200117154201TC25GENIChomozygous116671036
8117155022117155023GA16GENIChomozygous116671038
8117155793117155794AG21GENIChomozygous116671040
8117156147117156148TC30GENIChomozygous116671042
8117156238117156239GA24GENIChomozygous116671044
8117156696117156697GA24GENIChomozygous116671046
8117161298117161299CT9GENIChomozygous116671052
8117164752117164753GA21GENIChomozygous116671054
8117166879117166880CT32GENIChomozygous116671056
8117167217117167218AG17GENIChomozygous116671058
8117167561117167562GA21GENIChomozygous116671060
8117167628117167629AG19GENIChomozygous116671062
8117168124117168125GA24GENIChomozygous116671064
8117169086117169087TC25GENIChomozygous116671066