chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	171518933	171518934	G	A	23	GENIC	possibly homozygous	109167890
1	171538745	171538746	A	T	22	GENIC	homozygous	109167896
1	171539016	171539017	A	G	29	GENIC	homozygous	108378204
1	171546974	171546975	A	T	16	GENIC	homozygous	108378219
1	171549137	171549138	G	A	24	GENIC	homozygous	108378221
1	171549564	171549565	A	G	32	GENIC	homozygous	108378223
1	171549976	171549977	A	G	31	GENIC	homozygous	108378225
1	171550183	171550184	G	A	22	GENIC	possibly homozygous	108378227
1	171550803	171550804	T	C	18	GENIC	homozygous	108378229
1	171557058	171557059	T	A	26	GENIC	homozygous	109167904
1	171557804	171557805	G	A	14	GENIC	possibly homozygous	109167906
1	171561779	171561780	A	G	38	GENIC	homozygous	109167920
1	171562726	171562727	G	A	27	GENIC	homozygous	109167922
1	171563071	171563072	T	C	25	GENIC	homozygous	108378240
1	171564559	171564560	G	T	29	GENIC	homozygous	109167924
1	171564723	171564724	C	T	29	GENIC	possibly homozygous	109167926
1	171565121	171565122	A	C	27	GENIC	homozygous	109167928
1	171565675	171565676	C	T	27	GENIC	homozygous	109167930
1	171565997	171565998	T	C	27	GENIC	homozygous	109167932
1	171566301	171566302	C	T	33	GENIC	homozygous	109167934
1	171566629	171566630	T	C	27	GENIC	homozygous	109167936
1	171566660	171566661	A	G	24	GENIC	homozygous	109167938