chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59506110	59506111	C	CTCTG	17	GENIC	possibly homozygous	51465665
10	59507089	59507090	C	G	5	GENIC	homozygous	52319582
10	59507946	59507947	C	T	35	GENIC	homozygous	52062337
10	59509265	59509275	GTGTGTGTGT	----------	11	GENIC	homozygous	51897721
10	59509411	59509413	TT	--	9	GENIC	heterozygous	51663532
10	59509412	59509413	T	-	9	GENIC	heterozygous	51663534
10	59509707	59509708	C	CA	3	GENIC	homozygous	51897725
10	59509812	59509813	C	A	31	GENIC	homozygous	51465670
10	59512766	59512767	T	TTTATTA	2	GENIC	homozygous	52724295
10	59514922	59514923	T	TAA	14	GENIC	heterozygous	51465677
10	59514922	59514923	T	TA	14	GENIC	possibly homozygous	51663561
10	59515518	59515519	C	CAA	15	GENIC	heterozygous	51465678
10	59515518	59515519	C	CAAA	15	GENIC	heterozygous	51465679
10	59515518	59515519	C	CA	15	GENIC	heterozygous	52379114
10	59517426	59517427	T	C	20	GENIC	homozygous	51465681
10	59524101	59524102	A	G	25	GENIC	homozygous	51465688
10	59525601	59525602	G	T	29	GENIC	homozygous	52062339
10	59526259	59526260	C	A	33	GENIC	homozygous	52062341
10	59526695	59526696	C	T	27	GENIC	homozygous	52062343
10	59528292	59528293	T	C	30	GENIC	homozygous	51465689