chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62999191	62999192	G	A	14	GENIC	homozygous	117997772
10	63002932	63002933	A	T	7	GENIC	homozygous	117012939
10	63026817	63026818	A	G	69	GENIC	heterozygous	116614641
10	63026921	63026922	G	A	31	GENIC	heterozygous	116614643
10	63029686	63029687	C	T	36	GENIC	heterozygous	118041166
10	63029695	63029696	G	A	37	GENIC	heterozygous	118041167
10	63029700	63029701	C	T	38	GENIC	heterozygous	118041168
10	63029710	63029711	G	A	40	GENIC	heterozygous	118041169
10	63029718	63029719	C	A	38	GENIC	heterozygous	118041170
10	63029726	63029727	T	C	38	GENIC	heterozygous	118041171
10	63033820	63033821	G	T	8	GENIC	homozygous	117997916
10	63033832	63033833	A	G	4	GENIC	homozygous	117997918
10	63033835	63033836	G	A	4	GENIC	homozygous	117997920
10	63033842	63033843	C	T	4	GENIC	homozygous	118123911
10	63033843	63033844	G	A	4	GENIC	homozygous	117997921
10	63033846	63033847	T	A	4	GENIC	homozygous	117997923
10	63033849	63033850	T	C	4	GENIC	homozygous	117997925
10	63033858	63033859	G	A	4	GENIC	homozygous	117997927
10	63041069	63041070	A	C	4	GENIC	homozygous	117997931
10	63041260	63041261	C	T	12	GENIC	homozygous	117997932