chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 105016886 105016887 A C 21 GENIC homozygous 963189143 2 105019640 105019641 A G 25 GENIC homozygous 963189144 2 105020239 105020240 C T 19 GENIC homozygous 963189145 2 105020353 105020354 G A 13 GENIC homozygous 963189146 2 105027043 105027044 A G 12 GENIC homozygous 963189147 2 105027251 105027252 G T 18 GENIC homozygous 963189148 2 105027389 105027390 C G 19 GENIC homozygous 963189149 2 105029318 105029319 C A 30 GENIC homozygous 963189150 2 105029712 105029713 T C 18 GENIC homozygous 963189151 2 105039036 105039037 A T 9 GENIC heterozygous 963189152 2 105043493 105043494 C T 12 GENIC heterozygous 963189153 2 105045764 105045765 T G 19 GENIC homozygous 963189154