chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 111698989 111698990 G A 23 GENIC homozygous 967324894 8 111700490 111700491 T C 31 GENIC homozygous 967324895 8 111700575 111700576 T C 40 GENIC homozygous 967324896 8 111702284 111702285 G A 27 GENIC homozygous 967324897 8 111706168 111706169 G A 45 GENIC possibly homozygous 967324898 8 111706234 111706235 G A 31 GENIC homozygous 967324899 8 111706261 111706262 G A 30 GENIC homozygous 967324900 8 111706952 111706953 C T 35 GENIC homozygous 967324901 8 111708179 111708180 G A 47 GENIC possibly homozygous 967324902 8 111708481 111708482 T C 22 GENIC homozygous 967324903 8 111709172 111709173 G C 30 GENIC homozygous 967324904 8 111709376 111709377 G A 47 GENIC homozygous 967324905 8 111710507 111710508 A T 12 GENIC homozygous 967324906 8 111711762 111711763 G T 35 GENIC possibly homozygous 967324907 8 111713977 111713978 A G 19 GENIC homozygous 967324908 8 111716278 111716279 T G 27 GENIC homozygous 967324909 8 111718542 111718543 G A 11 GENIC homozygous 967324910 8 111719885 111719886 A G 21 GENIC homozygous 967324911 8 111720114 111720115 G A 43 GENIC homozygous 967324912 8 111720827 111720828 C T 22 GENIC homozygous 967324913