chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39171659	39171660	T	C	25	GENIC	homozygous	51422590
10	39171765	39171766	G	A	20	GENIC	homozygous	51422591
10	39172153	39172154	G	A	36	GENIC	homozygous	51422592
10	39172971	39172972	G	T	27	GENIC	possibly homozygous	51422593
10	39172980	39172981	G	T	26	GENIC	heterozygous	51634705
10	39172991	39172992	G	T	24	GENIC	possibly homozygous	51422594
10	39173144	39173145	T	C	28	GENIC	homozygous	51422595
10	39173312	39173313	C	T	29	GENIC	homozygous	51422596
10	39179884	39179885	G	A	29	GENIC	homozygous	51422597
10	39180201	39180202	A	ATGCTC	10	GENIC	homozygous	51422598
10	39180465	39180466	C	T	44	GENIC	homozygous	51422599
10	39182344	39182345	C	A	30	GENIC	homozygous	51422600
10	39184031	39184039	AGCCTGTC	--------	7	GENIC	homozygous	51422601
10	39184716	39184717	G	-	28	GENIC	homozygous	51422602
10	39179988	39179989	G	T	33	GENIC	possibly homozygous	52043630