chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	167183382	167183383	G	C	20	GENIC	heterozygous	59202643
2	167183418	167183419	T	C	26	GENIC	homozygous	59202644
2	167183740	167183741	T	TA	34	GENIC	homozygous	59202645
2	167183849	167183850	A	G	59	GENIC	homozygous	59202646
2	167183904	167183905	A	C	55	GENIC	homozygous	59202647
2	167184073	167184074	G	A	50	GENIC	homozygous	59202648
2	167184516	167184517	C	T	43	GENIC	homozygous	59202649
2	167184800	167184801	A	G	38	GENIC	homozygous	59202650
2	167185137	167185138	G	C	49	GENIC	possibly homozygous	59202651
2	167185476	167185477	G	T	39	GENIC	homozygous	59202652
2	167185547	167185555	GATTTTGT	--------	7	GENIC	heterozygous	59202653
2	167185547	167185548	G	-	7	GENIC	heterozygous	59202654
2	167185556	167185589	TGGTGTGAAAACAATTCCTAGATTTCTAGACAG	---------------------------------	2	GENIC	homozygous	59202655
2	167186142	167186143	C	T	54	GENIC	homozygous	59202656
2	167186442	167186443	G	A	43	GENIC	homozygous	59202657
2	167187184	167187185	T	C	41	GENIC	homozygous	59202658
2	167187205	167187206	G	A	37	GENIC	homozygous	59202659
2	167187280	167187281	T	C	37	GENIC	homozygous	59202660