chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	73784852	73784853	C	A	94	GENIC	homozygous	111927741
3	73784917	73784918	C	T	84	GENIC	homozygous	111927743
3	73785016	73785017	A	G	71	GENIC	homozygous	111927745
3	73785240	73785241	C	T	48	GENIC	homozygous	111927747
3	73785293	73785294	T	C	42	GENIC	homozygous	111927749
3	73785416	73785417	T	C	49	GENIC	homozygous	111927751
3	73785546	73785547	C	G	61	GENIC	possibly homozygous	111927753
3	73785598	73785599	A	G	52	GENIC	homozygous	111927755
3	73785618	73785619	T	A	50	GENIC	homozygous	111927757
3	73785832	73785833	G	A	39	GENIC	homozygous	111927759
3	73786252	73786253	G	T	54	GENIC	homozygous	111927761
3	73786259	73786260	T	C	51	GENIC	homozygous	111927763
3	73786354	73786355	G	A	48	GENIC	homozygous	111927765
3	73786456	73786457	C	T	55	GENIC	homozygous	111927767
3	73786979	73786980	A	G	55	GENIC	homozygous	111927769
3	73787080	73787081	G	A	54	GENIC	homozygous	111927771
3	73787135	73787136	G	A	67	GENIC	homozygous	111927773
3	73787581	73787582	G	T	63	GENIC	homozygous	111927775
3	73787714	73787715	A	T	70	GENIC	possibly homozygous	111927777
3	73787806	73787807	G	C	52	GENIC	homozygous	111927779
3	73787972	73787973	T	C	61	GENIC	homozygous	111927781
3	73788156	73788157	C	A	45	GENIC	homozygous	111927783
3	73788193	73788194	T	C	62	GENIC	homozygous	111927785
3	73788464	73788465	G	A	42	GENIC	possibly homozygous	111927787
3	73788659	73788660	A	T	52	GENIC	homozygous	111927789