chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108870395	108870396	A	G	37	GENIC	homozygous	51597808
10	108870530	108870531	A	G	33	GENIC	homozygous	51597810
10	108870919	108870920	G	A	24	GENIC	homozygous	51597812
10	108871175	108871179	CAAT	----	18	GENIC	homozygous	51597814
10	108871356	108871357	A	G	32	GENIC	homozygous	51597817
10	108872197	108872198	G	A	36	GENIC	homozygous	51597819
10	108873327	108873328	T	C	31	GENIC	homozygous	51597821
10	108873632	108873633	T	-	36	GENIC	possibly homozygous	51597822
10	108873691	108873692	G	A	27	GENIC	homozygous	51597824
10	108873818	108873819	A	G	30	GENIC	homozygous	51597826
10	108874079	108874080	T	TG	34	GENIC	homozygous	51597827
10	108874136	108874137	C	T	27	GENIC	homozygous	51597829
10	108874584	108874585	T	C	21	GENIC	homozygous	51597830
10	108874701	108874702	G	A	42	GENIC	homozygous	51597832
10	108876109	108876110	G	A	37	GENIC	homozygous	51597834
10	108876551	108876552	A	C	31	GENIC	possibly homozygous	51597836