chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108650764586507646AG14GENICpossibly homozygous51528128
108650851186508512T-14GENIChomozygous51921235
108650952486509525GA74GENIChomozygous51528134
108651098986510990TC54GENIChomozygous51921237
108651168286511683TG42GENICpossibly homozygous51528137
108651242386512424AT37GENIChomozygous51528138
108651417486514175GA64GENIChomozygous51528139
108651580386515804A-39GENIChomozygous51921239
108651602286516023AG62GENIChomozygous51921241
108651646286516463T-48GENIChomozygous51921243
108651660686516607CT35GENIChomozygous51921245
108651729886517299CG48GENIChomozygous51921247
108651749186517492GGA22GENIChomozygous51921249
108651751586517521AAAAGG------19GENICheterozygous51528144
108651772986517730GT61GENIChomozygous51921251
108651783886517839TC39GENIChomozygous51528145
108651820786518208AG46GENIChomozygous51921252
108651889986518900CT28GENIChomozygous52263203