chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105417358	105417359	A	-	8	GENIC	heterozygous	51761062
10	105418503	105418504	G	-	17	GENIC	heterozygous	51999348
10	105430136	105430137	C	CT	39	GENIC	homozygous	51589962
10	105425293	105425294	T	-	32	GENIC	possibly homozygous	51589948
10	105425297	105425298	G	-	34	GENIC	possibly homozygous	51589950
10	105425877	105425878	C	CT	2	GENIC	heterozygous	51589952
10	105426633	105426634	A	C	52	GENIC	heterozygous	51589954
10	105426660	105426661	G	A	63	GENIC	heterozygous	51589956
10	105426953	105426954	T	C	42	GENIC	heterozygous	51589960
10	105425878	105425879	T	-	2	GENIC	heterozygous	51951657
10	105430178	105430179	T	C	41	GENIC	homozygous	51589964
10	105430235	105430236	G	GC	31	GENIC	homozygous	51589966