chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 50749662 50749663 A C 31 GENIC homozygous 970712347 13 50750596 50750597 T C 18 GENIC homozygous 970712348 13 50751286 50751287 T C 24 GENIC homozygous 970712349 13 50752145 50752146 A G 27 GENIC homozygous 970712350 13 50752726 50752727 C G 22 GENIC homozygous 970712351 13 50753143 50753144 G A 36 GENIC homozygous 970712352 13 50756908 50756909 C G 34 GENIC homozygous 970712353 13 50757108 50757109 G A 29 GENIC homozygous 970712354 13 50757883 50757884 C T 29 GENIC homozygous 970712355 13 50757963 50757964 G A 39 GENIC homozygous 970712356 13 50759524 50759525 T C 40 GENIC homozygous 970712357 13 50762372 50762373 G C 39 GENIC homozygous 970712358