chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	45350351	45350351		A	13	GENIC	possibly homozygous	146462135
8	45351182	45351183	A	G	25	GENIC	homozygous	138325946
8	45351961	45351962	C	T	23	GENIC	homozygous	138325947
8	45351980	45351981	G	A	19	GENIC	homozygous	138325948
8	45352032	45352033	A	G	12	GENIC	homozygous	140897617
8	45352358	45352359	T	G	19	GENIC	homozygous	138325949
8	45354644	45354645	T	C	21	GENIC	homozygous	138325952
8	45355170	45355171	G	A	17	GENIC	homozygous	138325953
8	45355664	45355665	G	A	11	GENIC	homozygous	138325954
8	45355998	45356005	GTGTGTG		12	GENIC	possibly homozygous	146462136
8	45356111	45356112	T	C	15	GENIC	homozygous	138325955
8	45356620	45356621	T	C	16	GENIC	homozygous	138325956
8	45356888	45356889	G	A	17	GENIC	homozygous	146465776
8	45352308	45352309	C		21	GENIC	homozygous	403933718
8	45352308	45352309	C	A	21	GENIC	heterozygous	403933719
8	45354309	45354310	T		14	GENIC	homozygous	138243650
8	45356067	45356093	TGTGAGTGTGTGTGTGTGTGTGTGTG		13	GENIC	homozygous	138243651
8	45353456	45353457	C	T	20	GENIC	homozygous	146465773
8	45355130	45355131	T	A	19	GENIC	homozygous	146465774
8	45355515	45355516	C	T	19	GENIC	homozygous	146465775
8	45357546	45357547	G	A	13	GENIC	homozygous	146465777
8	45357799	45357800	T	G	21	GENIC	homozygous	146465778
8	45358815	45358815		A	13	GENIC	homozygous	138243652