chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89165379	89165380	C	CAG	18	GENIC	homozygous	51536696
10	89166059	89166060	T	C	14	GENIC	homozygous	51536697
10	89166472	89166473	G	A	21	GENIC	homozygous	51732107
10	89167400	89167401	A	G	26	GENIC	homozygous	51536699
10	89167523	89167524	C	T	25	GENIC	homozygous	51732115
10	89167673	89167674	A	G	27	GENIC	homozygous	51536700
10	89167887	89167888	A	-	11	GENIC	possibly homozygous	51732119
10	89168534	89168535	T	C	29	GENIC	homozygous	51536701
10	89168701	89168702	C	T	16	GENIC	homozygous	51732121
10	89169210	89169211	G	A	22	GENIC	homozygous	51536702
10	89169749	89169750	G	C	23	GENIC	homozygous	51536703
10	89169955	89169956	G	GA	24	GENIC	homozygous	51732123
10	89169987	89169988	C	-	17	GENIC	homozygous	51732125
10	89170380	89170381	C	T	21	GENIC	homozygous	51536704
10	89170454	89170455	C	A	31	GENIC	homozygous	51732127
10	89170625	89170626	T	G	29	GENIC	homozygous	51536705
10	89170913	89170914	A	AG	10	GENIC	heterozygous	51732129