chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 121378344 121378345 G C 149 GENIC possibly homozygous 801555167 1 121378349 121378350 G A 158 GENIC heterozygous 801555168 1 121378494 121378495 G A 110 GENIC possibly homozygous 801555169 1 121378511 121378512 C A 244 GENIC possibly homozygous 801555170 1 121378575 121378576 T A 231 GENIC heterozygous 801555171 1 121378576 121378577 G T 232 GENIC heterozygous 801555172 1 121378577 121378578 G T 233 GENIC heterozygous 801555173 1 121378600 121378601 T A 184 GENIC possibly homozygous 801555174 1 121378609 121378610 G A 206 GENIC heterozygous 801555175 1 121378632 121378633 A G 115 GENIC homozygous 801555176 1 121378646 121378647 C A 171 GENIC heterozygous 801555177 1 121378667 121378668 G T 190 GENIC heterozygous 801555178 1 121378683 121378684 T A 202 GENIC heterozygous 801555179 1 121378728 121378729 A T 189 GENIC possibly homozygous 801555180 1 121378764 121378765 T A 213 GENIC heterozygous 801555181 1 121378846 121378847 T G 75 GENIC possibly homozygous 801555182 1 121378924 121378925 C T 51 GENIC possibly homozygous 801555183 1 121383593 121383594 C T 8 GENIC homozygous 801555184 1 121383598 121383599 T A 8 GENIC homozygous 801555185 1 121383614 121383615 T C 7 GENIC possibly homozygous 801555186 1 121383631 121383632 T A 6 GENIC homozygous 801555187