chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 111735654 111735655 C T 31 GENIC homozygous 552788122 3 111735804 111735805 T C 38 GENIC homozygous 552788123 3 111735827 111735828 T G 43 GENIC homozygous 552788124 3 111735906 111735907 T A 31 GENIC homozygous 552788125 3 111736258 111736259 G A 25 GENIC homozygous 552788126 3 111736750 111736751 C CA 23 GENIC homozygous 702605177 3 111737037 111737038 G A 20 GENIC homozygous 552788127 3 111737191 111737192 G C 21 GENIC homozygous 552788128 3 111737599 111737600 C CT 14 GENIC possibly homozygous 702605178 3 111737790 111737791 G A 30 GENIC homozygous 552788129 3 111739416 111739417 A G 25 GENIC homozygous 552788130 3 111739796 111739797 C T 31 GENIC homozygous 552788131 3 111740272 111740274 TC -- 29 GENIC homozygous 702605179 3 111740639 111740640 A C 30 GENIC homozygous 552788132 3 111740640 111740641 T C 31 GENIC homozygous 552788133 3 111741074 111741075 C T 35 GENIC homozygous 552788134 3 111741114 111741115 C CACTT 39 GENIC homozygous 702605180 3 111741259 111741260 A G 33 GENIC homozygous 552788135 3 111741585 111741586 T C 31 GENIC homozygous 552788136 3 111741761 111741762 G A 25 GENIC homozygous 552788137 3 111741865 111741866 A T 17 GENIC homozygous 552788138 3 111742001 111742002 G GTTTTTTTTTTTTTTTTTTTTTTT 6 GENIC heterozygous 702605181 3 111742340 111742341 C T 21 GENIC homozygous 552788139