chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64061143	64061144	C	T	34	GENIC	homozygous	116791967
10	64061392	64061393	G	A	22	GENIC	homozygous	116791969
10	64062364	64062365	T	C	35	GENIC	homozygous	116616812
10	64062633	64062634	C	A	34	GENIC	homozygous	116791971
10	64063507	64063508	T	C	46	GENIC	homozygous	116616814
10	64063642	64063643	A	G	29	GENIC	homozygous	116616816
10	64064491	64064492	T	G	41	GENIC	homozygous	116616818
10	64064673	64064674	T	G	33	GENIC	possibly homozygous	116941047
10	64064743	64064744	C	T	26	GENIC	homozygous	116791973
10	64065143	64065144	T	C	43	GENIC	homozygous	116616822
10	64065289	64065290	G	A	33	GENIC	homozygous	116791975
10	64065636	64065637	G	A	28	GENIC	homozygous	116616826
10	64066459	64066460	T	C	22	GENIC	homozygous	116616828
10	64067228	64067229	T	C	29	GENIC	homozygous	117998350
10	64067498	64067499	G	A	41	GENIC	homozygous	116616832
10	64067763	64067764	C	T	27	GENIC	homozygous	116616834
10	64067826	64067827	C	A	27	GENIC	homozygous	116616836
10	64067964	64067965	G	T	35	GENIC	homozygous	116616838
10	64068453	64068454	G	A	53	GENIC	homozygous	116616840
10	64068543	64068544	C	T	33	GENIC	homozygous	116616842
10	64068575	64068576	G	A	28	GENIC	homozygous	116616844
10	64069527	64069528	T	C	33	GENIC	homozygous	116616848
10	64070604	64070605	C	T	41	GENIC	homozygous	116791977
10	64070820	64070821	A	G	28	GENIC	homozygous	116616852