chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 50749662 50749663 A C 27 GENIC homozygous 795492344 13 50750596 50750597 T C 21 GENIC homozygous 795492345 13 50751286 50751287 T C 46 GENIC homozygous 795492346 13 50752145 50752146 A G 35 GENIC homozygous 795492347 13 50752726 50752727 C G 56 GENIC homozygous 795492348 13 50753143 50753144 G A 42 GENIC homozygous 795492349 13 50753890 50753891 G A 21 GENIC possibly homozygous 795492350 13 50756908 50756909 C G 41 GENIC homozygous 795492351 13 50757108 50757109 G A 38 GENIC homozygous 795492352 13 50757883 50757884 C T 36 GENIC homozygous 795492353 13 50757963 50757964 G A 41 GENIC possibly homozygous 795492354 13 50759524 50759525 T C 35 GENIC homozygous 795492355 13 50760830 50760831 C G 19 GENIC heterozygous 795492356 13 50760895 50760896 G C 32 GENIC homozygous 795492357 13 50762372 50762373 G C 32 GENIC homozygous 795492358 13 50763735 50763736 A G 31 GENIC homozygous 795492359 13 50765244 50765245 G A 22 GENIC homozygous 795492360 13 50765282 50765283 T A 30 GENIC homozygous 795492361 13 50769706 50769707 G C 11 GENIC homozygous 795492362 13 50769716 50769717 C G 12 GENIC possibly homozygous 795492363