chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430686130430687TG48INTERGENIChomozygous780887578
7130431011130431012GC36INTERGENIChomozygous780887579
7130432419130432420CA56GENICpossibly homozygous780887580
7130433453130433454CA67GENIChomozygous780887581
7130435479130435480AG66GENIChomozygous780887582
7130435663130435664GC40GENIChomozygous780887583
7130435821130435822TC63GENIChomozygous780887584
7130436509130436510AG56GENIChomozygous780887585
7130436753130436754CT54GENICpossibly homozygous780887586
7130436895130436896AG52GENIChomozygous780887587
7130436928130436929AG42GENIChomozygous780887588
7130439443130439444TC51GENIChomozygous780887589
7130439815130439816GA61GENIChomozygous780887590