chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89165379	89165380	C	CAG	15	GENIC	homozygous	51536696
10	89165788	89165797	GGCCTCGTC	---------	2	GENIC	homozygous	51925447
10	89166059	89166060	T	C	6	GENIC	heterozygous	51536697
10	89167399	89167400	C	G	2	GENIC	homozygous	51925453
10	89167400	89167401	A	G	2	GENIC	homozygous	51536699
10	89167673	89167674	A	G	18	GENIC	possibly homozygous	51536700
10	89168430	89168431	G	A	23	GENIC	homozygous	51925459
10	89168534	89168535	T	C	18	GENIC	homozygous	51536701
10	89169210	89169211	G	A	14	GENIC	homozygous	51536702
10	89169749	89169750	G	C	21	GENIC	homozygous	51536703
10	89169987	89169988	C	-	2	GENIC	homozygous	51732125
10	89170380	89170381	C	T	8	GENIC	homozygous	51536704
10	89170625	89170626	T	G	22	GENIC	possibly homozygous	51536705
10	89170913	89170914	A	AG	2	GENIC	heterozygous	51732129