chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	5009945	5009945		A	16	GENIC	homozygous	128784524
10	5009953	5009953		G	22	GENIC	homozygous	128784525
10	5009962	5009962		A	25	GENIC	homozygous	128784526
10	5009980	5009982	CC		34	GENIC	homozygous	128784527
10	5009987	5009988	G		34	GENIC	homozygous	128784528
10	5009998	5010000	GC		43	GENIC	homozygous	128784529
10	5021049	5021050	G	T	6	GENIC	homozygous	116975236
10	5032086	5032087	A	G	19	GENIC	homozygous	116474013
10	5037330	5037331	G	A	6	GENIC	heterozygous	128864818
10	5037372	5037373	G	A	4	GENIC	heterozygous	128864819
10	5038133	5038134	A	C	6	GENIC	heterozygous	117977885
10	5038496	5038497	A		3	GENIC	homozygous	128784534
10	5037861	5037862	A	G	4	GENIC	heterozygous	133760786
10	5096033	5096034	C	A	61	GENIC	homozygous	116474170
10	5096042	5096043	G	C	60	GENIC	homozygous	116474172
10	5096043	5096044	T	A	59	GENIC	homozygous	116474174
10	5096045	5096046	T	C	59	GENIC	homozygous	116474176
10	5096046	5096047	A	T	59	GENIC	homozygous	116474178
10	5096048	5096049	G	C	59	GENIC	homozygous	116474180
10	5096179	5096180	C	T	53	GENIC	homozygous	116474182
10	5096181	5096182	C	A	55	GENIC	homozygous	116474184
10	5096183	5096183		AC	56	GENIC	homozygous	128784552