chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	11002766	11002766		G	38	GENIC	homozygous	142195980
10	11003780	11003781	C	G	53	GENIC	homozygous	142213466
10	11004692	11004693	T	C	42	GENIC	homozygous	142213467
10	11005139	11005140	G	A	61	GENIC	homozygous	142213468
10	11007126	11007129	AAG		35	GENIC	homozygous	142195981
10	11008675	11008676	C	T	65	GENIC	homozygous	142213469
10	11009309	11009310	A	T	29	GENIC	homozygous	142213470
10	11009352	11009353	T	C	15	GENIC	homozygous	142213471
10	11009555	11009556	C	T	14	GENIC	homozygous	142213472
10	11009723	11009724	C		18	GENIC	homozygous	142195982
10	11010624	11010625	A	G	55	GENIC	homozygous	142213473
10	11012348	11012349	C	T	51	GENIC	homozygous	142213474
10	11012930	11012931	T	C	58	GENIC	homozygous	142213475
10	11014272	11014272		CTC	47	GENIC	homozygous	142195983
10	11015045	11015046	G	T	55	GENIC	homozygous	142213476
10	11015049	11015050	C	G	54	GENIC	homozygous	142213477
10	11015772	11015772		G	43	GENIC	homozygous	142195984
10	11008133	11008147	TTTTTTTTTTTGTT		16	GENIC	homozygous	147571685
10	11008161	11008162	T	G	19	GENIC	possibly homozygous	147575718
10	11017494	11017551	ACACACACACCACACACACCACACACACACACACACCACACCACACACCACACACTG		14	GENIC	homozygous	147571686
10	11017579	11017580	A		18	GENIC	homozygous	147571687
10	11017591	11017593	AC		21	GENIC	possibly homozygous	147571688
10	11017602	11017609	CACACAC		19	GENIC	possibly homozygous	147571689
10	11018388	11018389	T	C	49	GENIC	homozygous	142213478
10	11017589	11017590	A	C	20	GENIC	homozygous	403631667
10	11009708	11009709	G		13	GENIC	heterozygous	403276156
10	11009708	11009709	G	T	13	GENIC	heterozygous	403276157