chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	103073151	103073152	C	T	58	GENIC	homozygous	142266088
10	103073198	103073199	G	A	62	GENIC	homozygous	142266089
10	103073621	103073622	T	C	41	GENIC	homozygous	142266096
10	103073737	103073738	G	C	61	GENIC	homozygous	142266099
10	103073768	103073769	T	G	58	GENIC	homozygous	148922847
10	103075251	103075252	G	A	41	GENIC	homozygous	148922848
10	103076078	103076079	T	C	44	GENIC	homozygous	142266113
10	103076260	103076261	G	A	59	GENIC	homozygous	148922849
10	103074356	103074359	TGT		38	GENIC	homozygous	142207769
10	103074262	103074262		AATTTCT	42	GENIC	homozygous	148919114
10	103074263	103074263		CCTCA	42	GENIC	homozygous	148919115
10	103075030	103075036	CCCCAC		31	GENIC	homozygous	148919116
10	103076866	103076867	A	G	27	GENIC	homozygous	142266116
10	103077155	103077156	G	A	42	GENIC	homozygous	142266118
10	103077259	103077260	A	G	48	GENIC	homozygous	148922850
10	103077356	103077357	T	C	43	GENIC	homozygous	148922851
10	103077482	103077483	A	G	32	GENIC	homozygous	148922852
10	103077702	103077703	G	A	45	GENIC	homozygous	148922853
10	103075418	103075419	T	C	50	GENIC	homozygous	154672715
10	103075418	103075419	T		50	GENIC	heterozygous	404017648