chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	167181188	167181189	A	G	34	GENIC	homozygous	108357618
1	167181468	167181469	A	G	19	GENIC	homozygous	109343141
1	167183609	167183610	T	C	34	GENIC	homozygous	109343143
1	167184176	167184177	C	A	36	GENIC	homozygous	109343145
1	167184389	167184390	A	G	34	GENIC	homozygous	108357619
1	167186792	167186793	T	G	29	GENIC	homozygous	108357620
1	167187596	167187597	C	T	23	GENIC	homozygous	109343147
1	167188910	167188911	C	T	23	GENIC	homozygous	109343149
1	167189616	167189617	T	G	51	GENIC	possibly homozygous	108357623
1	167189694	167189695	A	G	42	GENIC	possibly homozygous	108357624
1	167189758	167189759	A	G	29	GENIC	heterozygous	109343151
1	167189839	167189840	G	A	26	GENIC	heterozygous	109343153
1	167189887	167189888	A	G	13	GENIC	homozygous	109343155
1	167190028	167190029	A	G	32	GENIC	homozygous	108357625
1	167190748	167190749	G	A	41	GENIC	homozygous	108357628
1	167191072	167191073	A	G	31	GENIC	homozygous	108357630
1	167192105	167192106	G	T	29	GENIC	homozygous	108357631