chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	51672226	51672227	A		20	GENIC	heterozygous	403305996
11	51672226	51672227	A	G	20	GENIC	heterozygous	403305997
11	51674195	51674198	AAA		3	GENIC	heterozygous	141119470
11	51693116	51693117	T		44	GENIC	heterozygous	138888862
11	51693116	51693117	T	C	44	GENIC	heterozygous	154699970
11	51697064	51697064		CGTG	29	GENIC	homozygous	140905845
11	51697069	51697071	AT		19	GENIC	heterozygous	141038343
11	51697070	51697071	T	C	19	GENIC	heterozygous	403306000
11	51697070	51697071	T		19	GENIC	heterozygous	403306001
11	51697082	51697083	T	C	19	GENIC	heterozygous	403306002
11	51697082	51697083	T		19	GENIC	heterozygous	403306003
11	51697086	51697087	T	C	19	GENIC	heterozygous	403306004
11	51697086	51697087	T		19	GENIC	heterozygous	403306005
11	51697098	51697099	T	C	22	GENIC	homozygous	138991747
11	51745500	51745501	A	G	25	GENIC	homozygous	144427366