chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 41863267 41863268 A G 17 GENIC homozygous 74992151 1 41863271 41863272 T C 17 GENIC homozygous 74992152 1 41863824 41863825 A G 17 GENIC homozygous 74992153 1 41863907 41863908 G C 17 GENIC homozygous 74992154 1 41864570 41864571 A G 6 GENIC homozygous 74992155 1 41864642 41864643 A G 6 GENIC homozygous 74992156 1 41864679 41864680 T G 3 GENIC homozygous 74992157 1 41864930 41864931 A T 5 GENIC homozygous 74992158 1 41864946 41864947 G A 9 GENIC homozygous 74992159 1 41864992 41864993 C T 11 GENIC homozygous 74992160 1 41865590 41865591 T A 23 GENIC homozygous 74992161 1 41865740 41865741 C T 14 GENIC heterozygous 74992162 1 41865750 41865751 C A 13 GENIC heterozygous 76678181 1 41865797 41865798 A C 6 GENIC homozygous 74992163 1 41865937 41865938 A G 10 GENIC homozygous 74992164 1 41866900 41866901 A T 11 GENIC homozygous 74992165 1 41867361 41867362 G C 35 GENIC homozygous 74992166 1 41867660 41867661 C G 23 GENIC homozygous 74992167 1 41867775 41867776 A G 21 GENIC homozygous 74992168 1 41867917 41867918 T G 14 GENIC homozygous 74992169 1 41868107 41868108 T C 11 GENIC homozygous 74992170 1 41868423 41868424 C A 17 GENIC homozygous 74992171 1 41868996 41868997 G A 12 GENIC homozygous 74992172 1 41869811 41869812 G C 13 GENIC homozygous 74992173 1 41870181 41870182 C A 7 GENIC possibly homozygous 75397110