chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 125175833 125175834 T C 36 GENIC homozygous 996616781 3 125177947 125177948 A G 23 GENIC homozygous 996616782 3 125178727 125178728 T C 16 GENIC homozygous 996616783 3 125179757 125179758 A C 33 GENIC homozygous 996616784 3 125182814 125182815 T C 28 GENIC homozygous 996616785 3 125183301 125183302 C T 23 GENIC homozygous 996616786 3 125183719 125183720 G A 39 GENIC homozygous 996616787 3 125189281 125189282 A T 35 GENIC homozygous 996616788 3 125189784 125189785 C T 24 GENIC homozygous 996616789 3 125190594 125190595 G A 35 GENIC homozygous 996616790 3 125192028 125192029 T A 40 GENIC homozygous 996616791 3 125192032 125192033 G T 39 GENIC homozygous 996616792 3 125203830 125203831 C T 34 GENIC homozygous 996616793 3 125205153 125205154 G A 23 GENIC homozygous 996616794 3 125207297 125207298 A G 20 GENIC homozygous 996616795 3 125208240 125208241 G A 24 GENIC homozygous 996616796 3 125208822 125208823 C T 26 GENIC homozygous 996616797 3 125209924 125209925 A G 21 GENIC homozygous 996616798 3 125210208 125210209 T C 21 GENIC homozygous 996616799 3 125212352 125212353 G A 22 GENIC homozygous 996616800