chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	57606780	57606781	T	C	53	GENIC	homozygous	116604013
10	57607287	57607288	C	T	42	GENIC	homozygous	116604015
10	57607512	57607513	A	G	42	GENIC	homozygous	116604017
10	57607882	57607883	T	C	49	GENIC	homozygous	116604019
10	57608009	57608010	G	C	52	GENIC	homozygous	116604021
10	57608046	57608047	A	G	52	GENIC	homozygous	116604023
10	57608479	57608480	G	C	35	GENIC	homozygous	116604025
10	57608515	57608516	A	G	32	GENIC	homozygous	116604027
10	57609262	57609263	C	T	50	GENIC	homozygous	116604029
10	57609431	57609432	T	C	50	GENIC	homozygous	116604031
10	57609934	57609935	G	C	40	GENIC	homozygous	116604033
10	57610838	57610839	A	G	60	GENIC	homozygous	116604035
10	57611034	57611035	G	A	52	GENIC	homozygous	116604037
10	57611039	57611040	G	A	55	GENIC	possibly homozygous	116604039
10	57611545	57611546	T	C	58	GENIC	possibly homozygous	116785601
10	57613674	57613675	G	A	29	GENIC	homozygous	116604041