chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 50749662 50749663 A C 31 GENIC homozygous 800127176 13 50750596 50750597 T C 18 GENIC homozygous 800127177 13 50751286 50751287 T C 25 GENIC homozygous 800127178 13 50752145 50752146 A G 27 GENIC homozygous 800127179 13 50752726 50752727 C G 24 GENIC homozygous 800127180 13 50753143 50753144 G A 36 GENIC homozygous 800127181 13 50753890 50753891 G A 21 GENIC possibly homozygous 800127182 13 50756908 50756909 C G 34 GENIC homozygous 800127183 13 50757108 50757109 G A 30 GENIC homozygous 800127184 13 50757883 50757884 C T 29 GENIC homozygous 800127185 13 50757963 50757964 G A 39 GENIC homozygous 800127186 13 50759524 50759525 T C 43 GENIC homozygous 800127187 13 50760895 50760896 G C 34 GENIC homozygous 800127188 13 50762372 50762373 G C 40 GENIC homozygous 800127189 13 50762703 50762704 A G 5 GENIC homozygous 800127190 13 50763735 50763736 A G 30 GENIC homozygous 800127191 13 50765244 50765245 G A 14 GENIC homozygous 800127192 13 50765282 50765283 T A 14 GENIC homozygous 800127193 13 50769706 50769707 G C 28 GENIC heterozygous 800127194 13 50769716 50769717 C G 26 GENIC heterozygous 800127195 13 50769779 50769780 C T 39 GENIC heterozygous 800127196