chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87307085	87307086	A	G	16	GENIC	homozygous	138842671
10	87307199	87307199		C	8	GENIC	possibly homozygous	138697196
10	87307300	87307303	TAA		9	GENIC	possibly homozygous	144857462
10	87310075	87310076	G	A	17	GENIC	homozygous	138842672
10	87310566	87310579	GGATCTCCGAGTG		15	GENIC	homozygous	138697197
10	87311022	87311022		TTCTC	14	GENIC	homozygous	138697198
10	87312390	87312391	A	G	19	GENIC	homozygous	138842673
10	87312784	87312785	T	C	16	GENIC	homozygous	138842674
10	87313222	87313223	T	C	9	GENIC	homozygous	138842675
10	87315713	87315713		G	16	GENIC	homozygous	138697199
10	87316028	87316029	G	A	24	GENIC	homozygous	138842678
10	87316648	87316649	C	A	15	GENIC	homozygous	138842679
10	87317936	87317937	A	G	22	GENIC	homozygous	143465413
10	87307302	87307303	A	T	9	GENIC	heterozygous	154658811
10	87307302	87307303	A		9	GENIC	possibly homozygous	403294045
10	87309681	87309682	G	A	22	GENIC	homozygous	143465411
10	87311018	87311019	G	A	14	GENIC	homozygous	143465412
10	87319805	87319806	G	A	14	GENIC	homozygous	143465414
10	87320322	87320323	T	C	23	GENIC	homozygous	138842681
10	87320650	87320651	A	G	15	GENIC	homozygous	138842682