chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 105016886 105016887 A C 53 GENIC homozygous 806378845 2 105019640 105019641 A G 50 GENIC homozygous 806378846 2 105020239 105020240 C T 52 GENIC homozygous 806378847 2 105020353 105020354 G A 62 GENIC homozygous 806378848 2 105020921 105020922 G A 60 GENIC heterozygous 806378849 2 105021105 105021106 C T 76 GENIC heterozygous 806378850 2 105021146 105021147 C G 116 GENIC heterozygous 806378851 2 105022210 105022211 C T 169 GENIC heterozygous 806378852 2 105022225 105022226 A C 169 GENIC heterozygous 806378853 2 105022564 105022565 A G 228 GENIC heterozygous 806378854 2 105022816 105022817 G A 75 GENIC heterozygous 806378855 2 105022821 105022822 C A 73 GENIC heterozygous 806378856 2 105022834 105022835 C G 80 GENIC heterozygous 806378857 2 105023244 105023245 A G 170 GENIC heterozygous 806378858 2 105024224 105024225 A C 90 GENIC heterozygous 806378859 2 105025607 105025608 T C 107 GENIC heterozygous 806378860 2 105025733 105025734 C A 154 GENIC heterozygous 806378861 2 105025770 105025771 G T 171 GENIC heterozygous 806378862 2 105025898 105025899 C T 102 GENIC heterozygous 806378863 2 105026507 105026508 G C 20 GENIC possibly homozygous 806378864 2 105026855 105026856 G A 5 GENIC homozygous 806378865 2 105027043 105027044 A G 38 GENIC homozygous 806378866 2 105027251 105027252 G T 51 GENIC possibly homozygous 806378867 2 105027389 105027390 C G 60 GENIC homozygous 806378868 2 105027563 105027564 A C 55 GENIC homozygous 806378869 2 105029318 105029319 C A 46 GENIC homozygous 806378870 2 105029712 105029713 T C 38 GENIC homozygous 806378871 2 105044760 105044761 A T 37 GENIC homozygous 806378872 2 105045764 105045765 T G 44 GENIC homozygous 806378873