chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 58509952 58509953 C A 51 GENIC possibly homozygous 792743287 2 58510337 58510338 A T 39 GENIC homozygous 792743288 2 58510357 58510358 T C 45 GENIC homozygous 792743289 2 58510921 58510922 C G 40 GENIC homozygous 792743290 2 58511819 58511820 A C 34 GENIC homozygous 792743291 2 58512633 58512634 G A 62 GENIC possibly homozygous 792743292 2 58514798 58514799 G A 42 GENIC homozygous 792743293 2 58515682 58515683 C T 22 GENIC homozygous 792743294 2 58518941 58518942 G A 42 GENIC homozygous 792743295 2 58519764 58519765 T C 38 GENIC homozygous 792743296 2 58519848 58519849 T A 45 GENIC homozygous 792743297 2 58520051 58520052 C T 41 GENIC homozygous 792743298 2 58520718 58520719 C T 44 GENIC homozygous 792743299 2 58522782 58522783 G A 33 GENIC homozygous 792743300 2 58522934 58522935 C T 33 GENIC homozygous 792743301 2 58523051 58523052 T C 31 GENIC homozygous 792743302 2 58526540 58526541 C T 56 GENIC homozygous 792743303 2 58531840 58531841 T C 39 GENIC homozygous 792743304 2 58531883 58531884 T C 36 GENIC homozygous 792743305 2 58533267 58533268 G A 42 GENIC homozygous 792743306