chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	186068834	186068835	T	G	37	GENIC	homozygous	59657721
4	186069030	186069031	A	G	29	GENIC	homozygous	59657722
4	186069935	186069936	T	TG	49	GENIC	homozygous	59657723
4	186070361	186070362	T	C	71	GENIC	homozygous	59657724
4	186071642	186071643	G	A	53	GENIC	homozygous	59657725
4	186072139	186072140	A	-	33	GENIC	homozygous	59657726
4	186072798	186072799	C	T	44	GENIC	homozygous	59657727
4	186073100	186073101	T	C	33	GENIC	homozygous	59657728
4	186073241	186073242	G	A	46	GENIC	homozygous	59657729
4	186073340	186073341	T	C	42	GENIC	homozygous	59657730
4	186073561	186073562	C	A	56	GENIC	homozygous	59657731
4	186076295	186076296	C	CTT	41	GENIC	homozygous	59657732
4	186078557	186078559	AA	--	7	GENIC	homozygous	58446340
4	186078723	186078724	T	C	20	GENIC	homozygous	59657733
4	186078727	186078728	C	A	18	GENIC	homozygous	59657734
4	186078870	186078871	C	T	19	GENIC	homozygous	59657735
4	186079062	186079063	C	T	30	GENIC	homozygous	59657736
4	186079538	186079539	C	A	57	GENIC	homozygous	59657737
4	186079539	186079540	C	T	58	GENIC	homozygous	59657738
4	186080622	186080623	A	G	43	GENIC	homozygous	59657741
4	186079722	186079723	G	A	53	GENIC	homozygous	59657739
4	186080058	186080059	C	T	27	GENIC	homozygous	59657740
4	186080791	186080792	G	C	56	GENIC	homozygous	59657742