chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89253765	89253766	A	G	11	GENIC	homozygous	51536901
10	89255596	89255597	A	-	12	GENIC	homozygous	53545123
10	89258417	89258418	T	C	7	GENIC	homozygous	53545124
10	89261732	89261733	G	A	17	GENIC	homozygous	53545125
10	89262963	89262964	T	-	20	GENIC	homozygous	51536919
10	89263540	89263544	GTCT	----	10	GENIC	homozygous	53545126
10	89273165	89273166	T	C	17	GENIC	homozygous	51536940
10	89275636	89275637	A	G	12	GENIC	homozygous	51536945
10	89275831	89275832	G	A	7	GENIC	homozygous	51536946
10	89275867	89275868	C	A	11	GENIC	homozygous	51536948
10	89278833	89278834	T	C	19	GENIC	homozygous	51536956
10	89278944	89278945	G	A	18	GENIC	homozygous	52574251
10	89279017	89279018	T	G	18	GENIC	homozygous	51536957
10	89279707	89279708	A	G	24	GENIC	homozygous	51536960
10	89279869	89279870	G	A	18	GENIC	homozygous	51925753
10	89281661	89281662	T	C	18	GENIC	homozygous	51536965