chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 1876193 1876194 T C 29 GENIC homozygous 801125136 20 1876354 1876355 T G 33 GENIC homozygous 801125137 20 1876408 1876409 A T 29 GENIC homozygous 801125138 20 1876430 1876431 A G 30 GENIC homozygous 801125139 20 1876595 1876596 G A 37 GENIC homozygous 801125140 20 1876761 1876762 T C 40 GENIC homozygous 801125141 20 1877105 1877106 T C 17 GENIC possibly homozygous 801125142 20 1877129 1877130 T C 20 GENIC homozygous 801125143 20 1877158 1877159 T C 20 GENIC homozygous 801125144 20 1877389 1877390 C T 28 GENIC homozygous 801125145 20 1877396 1877397 T C 25 GENIC homozygous 801125146 20 1877416 1877417 A G 30 GENIC homozygous 801125147 20 1877423 1877424 A G 31 GENIC homozygous 801125148 20 1877456 1877457 G A 27 GENIC homozygous 801125149 20 1877462 1877463 T C 26 GENIC homozygous 801125150 20 1877638 1877639 G T 32 GENIC possibly homozygous 801125151 20 1877756 1877757 A G 30 GENIC homozygous 801125152 20 1877946 1877947 G A 27 GENIC homozygous 801125153 20 1877950 1877951 T C 30 GENIC homozygous 801125154