chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89165379	89165380	C	CAG	20	GENIC	homozygous	51536696
10	89166059	89166060	T	C	30	GENIC	homozygous	51536697
10	89166472	89166473	G	A	29	GENIC	homozygous	51732107
10	89167400	89167401	A	G	27	GENIC	homozygous	51536699
10	89167523	89167524	C	T	21	GENIC	homozygous	51732115
10	89167673	89167674	A	G	21	GENIC	homozygous	51536700
10	89167886	89167887	C	CA	13	GENIC	heterozygous	52508091
10	89167887	89167888	A	-	13	GENIC	possibly homozygous	51732119
10	89168534	89168535	T	C	23	GENIC	homozygous	51536701
10	89168701	89168702	C	T	27	GENIC	homozygous	51732121
10	89169210	89169211	G	A	34	GENIC	homozygous	51536702
10	89169749	89169750	G	C	21	GENIC	homozygous	51536703
10	89169955	89169956	G	GA	18	GENIC	homozygous	51732123
10	89169987	89169988	C	-	20	GENIC	homozygous	51732125
10	89170380	89170381	C	T	20	GENIC	homozygous	51536704
10	89170454	89170455	C	A	19	GENIC	homozygous	51732127
10	89170625	89170626	T	G	35	GENIC	homozygous	51536705
10	89170913	89170914	A	AG	18	GENIC	possibly homozygous	51732129