chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89165379	89165380	C	CAG	14	GENIC	homozygous	51536696
10	89165788	89165797	GGCCTCGTC	---------	26	GENIC	homozygous	51925447
10	89166059	89166060	T	C	19	GENIC	homozygous	51536697
10	89167102	89167106	ACAG	----	9	GENIC	homozygous	51925449
10	89167399	89167400	C	G	23	GENIC	homozygous	51925453
10	89167400	89167401	A	G	22	GENIC	homozygous	51536699
10	89167128	89167130	AG	--	11	GENIC	possibly homozygous	51732109
10	89167673	89167674	A	G	28	GENIC	homozygous	51536700
10	89167816	89167817	T	TTTAGC	18	GENIC	homozygous	51925455
10	89167875	89167876	A	-	3	GENIC	homozygous	51925457
10	89167887	89167888	A	-	4	GENIC	heterozygous	51732119
10	89168430	89168431	G	A	22	GENIC	homozygous	51925459
10	89168534	89168535	T	C	29	GENIC	homozygous	51536701
10	89169210	89169211	G	A	28	GENIC	homozygous	51536702
10	89169749	89169750	G	C	38	GENIC	homozygous	51536703
10	89169955	89169956	G	GA	19	GENIC	homozygous	51732123
10	89169987	89169988	C	-	23	GENIC	possibly homozygous	51732125
10	89170380	89170381	C	T	28	GENIC	homozygous	51536704
10	89170625	89170626	T	G	24	GENIC	homozygous	51536705
10	89170913	89170914	A	AG	17	GENIC	possibly homozygous	51732129