chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85669163	85669163		TTTGG	38	GENIC	homozygous	143435006
10	85669672	85669673	A	G	65	GENIC	homozygous	138841598
10	85672498	85672498		CAGAGCATGAATCCC	59	GENIC	homozygous	138696754
10	85676779	85676780	C	T	59	GENIC	homozygous	138841602
10	85681140	85681141	A	G	55	GENIC	homozygous	138841607
10	85682460	85682461	A	G	47	GENIC	homozygous	138841608
10	85681108	85681109	C	T	51	GENIC	homozygous	143463253
10	85684430	85684430		G	62	GENIC	homozygous	138696756
10	85684962	85684963	A	G	58	GENIC	possibly homozygous	138841611
10	85685070	85685071	T	C	60	GENIC	homozygous	143463254
10	85685169	85685170	G	A	54	GENIC	possibly homozygous	143463255
10	85686453	85686454	T	C	69	GENIC	homozygous	138841620
10	85686688	85686689	C	G	69	GENIC	homozygous	143463256
10	85676883	85676884	G		44	GENIC	heterozygous	403293576
10	85683566	85683567	G	T	49	GENIC	possibly homozygous	154654774
10	85676883	85676884	G	T	44	GENIC	possibly homozygous	154654769