chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	51916700	51916701	A	G	15	GENIC	possibly homozygous	56889848
4	51916877	51916878	A	G	16	GENIC	heterozygous	56889850
4	51917125	51917126	A	T	11	GENIC	homozygous	56889852
4	51917138	51917139	T	A	6	GENIC	homozygous	56889854
4	51918770	51918771	A	-	2	GENIC	heterozygous	56889856
4	51919679	51919680	C	CT	3	GENIC	homozygous	56889862
4	51921114	51921115	T	C	1	GENIC	homozygous	57472457
4	51921121	51921122	C	CCA	1	GENIC	homozygous	56889864
4	51921742	51921743	C	T	18	GENIC	possibly homozygous	56889866
4	51921817	51921818	T	-	19	GENIC	homozygous	56889868
4	51922063	51922064	A	C	13	GENIC	heterozygous	56889870
4	51922167	51922168	T	C	4	GENIC	homozygous	56889872
4	51922206	51922207	C	T	1	GENIC	homozygous	56889874
4	51922229	51922231	AA	--	1	GENIC	homozygous	56889876
4	51923743	51923744	C	G	15	GENIC	possibly homozygous	56889882
4	51924133	51924134	G	A	14	GENIC	homozygous	56889884
4	51925296	51925297	T	C	9	GENIC	heterozygous	56889886
4	51925678	51925679	G	A	14	GENIC	homozygous	56889888
4	51926180	51926181	T	TA	12	GENIC	heterozygous	56889890
4	51926445	51926446	G	A	10	GENIC	homozygous	56889892
4	51926711	51926712	T	A	9	GENIC	homozygous	56889894
4	51926855	51926856	T	C	8	GENIC	homozygous	56889896
4	51928681	51928682	G	A	15	GENIC	homozygous	56889898
4	51928731	51928732	T	C	10	GENIC	homozygous	56889900
4	51929278	51929279	C	T	8	GENIC	homozygous	56889902
4	51931598	51931599	T	G	9	GENIC	homozygous	56889904
4	51932133	51932134	C	CA	12	GENIC	homozygous	56889906
4	51932681	51932682	T	C	8	GENIC	heterozygous	56889910
4	51934244	51934245	A	G	10	GENIC	homozygous	56889928
4	51934319	51934320	C	T	5	GENIC	heterozygous	56889930
4	51934329	51934330	G	T	6	GENIC	heterozygous	56889932
4	51935044	51935045	A	AT	2	GENIC	homozygous	56889934
4	51935127	51935128	A	C	16	GENIC	homozygous	56889936