chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121287280121287283CCC---20GENICpossibly homozygous54085881
7121287284121287285AT21GENICheterozygous54085882
7121287285121287288GGG---19GENIChomozygous54085883
7121287457121287458AG56GENIChomozygous54085884
7121288145121288146AG55GENIChomozygous54085885
7121288153121288154GC54GENIChomozygous54085886
7121288174121288175CT55GENIChomozygous54085887
7121288214121288215TC46GENIChomozygous54085888
7121288386121288387AG35GENIChomozygous54085889
7121288417121288418A-1GENIChomozygous54085890
7121288886121288887CT66GENIChomozygous54085891
7121289295121289296AG65GENIChomozygous54085892
7121289329121289330AG57GENIChomozygous54085893
7121289504121289505TC55GENIChomozygous54085894
7121289702121289703TC50GENIChomozygous54085895
7121289966121289967TG50GENICpossibly homozygous54085896
7121290229121290230CG35GENIChomozygous54085897
7121291272121291273GA62GENICpossibly homozygous54085898
7121291698121291699CG45GENIChomozygous54085899
7121291724121291725GT43GENIChomozygous54085900
7121291729121291730CG42GENIChomozygous54085901
7121291752121291753CA53GENIChomozygous54085902