chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 31719916 31719917 C T 15 GENIC homozygous 950630780 11 31720869 31720870 A G 34 GENIC homozygous 950630781 11 31721277 31721278 G A 17 GENIC possibly homozygous 950630782 11 31722705 31722706 T A 26 GENIC homozygous 950630783 11 31723854 31723855 G A 16 GENIC homozygous 950630784 11 31724160 31724161 C G 16 GENIC homozygous 950630785 11 31724703 31724704 A C 33 GENIC homozygous 950630786 11 31728249 31728250 C A 17 GENIC homozygous 950630787 11 31732574 31732575 C T 17 GENIC homozygous 950630788 11 31732769 31732770 T C 16 GENIC homozygous 950630789 11 31732799 31732800 A G 15 GENIC homozygous 950630790 11 31734460 31734461 A G 24 GENIC homozygous 950630791 11 31736309 31736310 G A 13 GENIC homozygous 950630792 11 31736800 31736801 T C 21 GENIC homozygous 950630793 11 31737948 31737949 A G 21 GENIC homozygous 950630794 11 31738577 31738578 C T 13 GENIC homozygous 950630795 11 31740577 31740578 G A 12 GENIC homozygous 950630796 11 31741852 31741853 G A 13 GENIC homozygous 950630797 11 31743622 31743623 A T 14 GENIC homozygous 950630798 11 31743917 31743918 G A 14 GENIC homozygous 950630799 11 31745524 31745525 C T 18 GENIC homozygous 950630800 11 31746642 31746643 C G 12 GENIC homozygous 950630801 11 31749282 31749283 A T 14 GENIC homozygous 950630802 11 31749631 31749632 G A 18 GENIC homozygous 950630803 11 31750179 31750180 G A 21 GENIC homozygous 950630804