chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	51693116	51693117	T		45	GENIC	heterozygous	138888862
11	51693116	51693117	T	C	45	GENIC	heterozygous	154699970
11	51697064	51697064		CGTG	37	GENIC	homozygous	140905845
11	51697069	51697071	AT		29	GENIC	heterozygous	141038343
11	51697070	51697071	T	C	29	GENIC	heterozygous	403306000
11	51697070	51697071	T		29	GENIC	heterozygous	403306001
11	51697082	51697083	T	C	29	GENIC	heterozygous	403306002
11	51697082	51697083	T		29	GENIC	heterozygous	403306003
11	51697086	51697087	T	C	29	GENIC	heterozygous	403306004
11	51697086	51697087	T		29	GENIC	heterozygous	403306005
11	51697098	51697099	T	C	40	GENIC	homozygous	138991747
11	51712576	51712577	C	T	12	GENIC	homozygous	403641089
11	51712576	51712577	C		12	GENIC	heterozygous	403641090