chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87307085	87307086	A	G	36	GENIC	homozygous	138842671
10	87307199	87307199		C	9	GENIC	possibly homozygous	138697196
10	87307300	87307303	TAA		26	GENIC	heterozygous	144857462
10	87310075	87310076	G	A	42	GENIC	homozygous	138842672
10	87310566	87310579	GGATCTCCGAGTG		57	GENIC	homozygous	138697197
10	87311022	87311022		TTCTC	58	GENIC	homozygous	138697198
10	87312390	87312391	A	G	62	GENIC	homozygous	138842673
10	87312784	87312785	T	C	50	GENIC	homozygous	138842674
10	87313222	87313223	T	C	42	GENIC	homozygous	138842675
10	87315713	87315713		G	42	GENIC	homozygous	138697199
10	87316028	87316029	G	A	57	GENIC	homozygous	138842678
10	87316648	87316649	C	A	49	GENIC	homozygous	138842679
10	87317936	87317937	A	G	55	GENIC	homozygous	143465413
10	87307302	87307303	A	T	26	GENIC	heterozygous	154658811
10	87307302	87307303	A		26	GENIC	possibly homozygous	403294045
10	87309681	87309682	G	A	43	GENIC	homozygous	143465411
10	87311018	87311019	G	A	58	GENIC	homozygous	143465412
10	87319805	87319806	G	A	57	GENIC	homozygous	143465414
10	87320322	87320323	T	C	60	GENIC	homozygous	138842681
10	87320650	87320651	A	G	51	GENIC	homozygous	138842682