chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430686130430687TG28GENIChomozygous955442260
7130432419130432420CA18GENIChomozygous955442261
7130433453130433454CA27GENICpossibly homozygous955442262
7130435479130435480AG18GENIChomozygous955442263
7130435663130435664GC10GENIChomozygous955442264
7130435821130435822TC30GENIChomozygous955442265
7130436509130436510AG32GENIChomozygous955442266
7130436753130436754CT20GENIChomozygous955442267
7130436895130436896AG30GENIChomozygous955442268
7130436928130436929AG25GENIChomozygous955442269
7130439443130439444TC17GENIChomozygous955442270
7130439815130439816GA36GENIChomozygous955442271