chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	80893184	80893185	T	C	43	GENIC	homozygous	111635909
3	80893198	80893199	G	T	46	GENIC	homozygous	111635910
3	80893743	80893744	C	T	36	GENIC	homozygous	111635911
3	80894023	80894024	T	C	16	GENIC	homozygous	111635912
3	80894657	80894658	T	G	29	GENIC	homozygous	111635913
3	80894858	80894859	T	C	19	GENIC	homozygous	111635914
3	80894871	80894872	T	C	26	GENIC	homozygous	111635915
3	80895990	80895991	G	A	61	GENIC	homozygous	111635916
3	80897140	80897141	T	C	32	GENIC	homozygous	111635917
3	80897591	80897592	A	T	57	GENIC	homozygous	111635918
3	80902590	80902591	G	A	53	GENIC	homozygous	111635919
3	80902915	80902916	G	A	26	GENIC	heterozygous	111635920
3	80906838	80906839	T	C	104	GENIC	possibly homozygous	111635921
3	80907360	80907361	C	T	121	GENIC	heterozygous	111635922
3	80908685	80908686	A	G	83	GENIC	homozygous	111635923
3	80908866	80908867	C	A	90	GENIC	heterozygous	111635924
3	80909006	80909007	C	T	38	GENIC	possibly homozygous	111635925
3	80909969	80909970	G	A	38	GENIC	homozygous	111635926
3	80914688	80914689	A	T	28	GENIC	homozygous	111635927
3	80915302	80915303	G	A	59	GENIC	homozygous	111635928
3	80919599	80919600	A	G	37	GENIC	homozygous	111635929
3	80923279	80923280	C	G	80	GENIC	homozygous	111635930
3	80930774	80930775	C	T	36	GENIC	homozygous	111635931
3	80931233	80931234	C	T	31	GENIC	possibly homozygous	111635932