chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	44620022	44620022		T	30	GENIC	homozygous	138681846
10	44620827	44620828	A	G	35	GENIC	homozygous	138782877
10	44621194	44621195	T	C	36	GENIC	homozygous	138782878
10	44622270	44622271	A	G	53	GENIC	homozygous	148749080
10	44622357	44622358	G	A	47	GENIC	homozygous	148749081
10	44623936	44623938	CA		45	GENIC	homozygous	138681848
10	44624237	44624238	G	A	47	GENIC	homozygous	148749082
10	44629613	44629614	G	A	46	GENIC	homozygous	148749083
10	44632201	44632202	G	T	55	GENIC	homozygous	148749084
10	44635152	44635153	G	A	33	GENIC	homozygous	148749085
10	44635498	44635499	A		42	GENIC	homozygous	138681856
10	44636563	44636564	A	G	37	GENIC	homozygous	138782892
10	44636624	44636625	G	A	41	GENIC	homozygous	148749086
10	44637702	44637703	T	A	4	GENIC	homozygous	148749087
10	44638987	44638988	C	T	35	GENIC	homozygous	148749088
10	44639182	44639183	T	C	50	GENIC	homozygous	138782893
10	44641821	44641822	T		49	GENIC	homozygous	138681859
10	44644957	44644958	A	T	62	GENIC	homozygous	148749089
10	44648219	44648220	A	T	35	GENIC	homozygous	138782905
10	44652376	44652377	C	T	37	GENIC	possibly homozygous	148749090
10	44625494	44625494		CATATGCTACTGTATCCAAT	32	GENIC	homozygous	148744644