chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	51697064	51697064		CGTG	11	GENIC	homozygous	140905845
11	51697069	51697071	AT		11	GENIC	homozygous	141038343
11	51697070	51697071	T	C	11	GENIC	heterozygous	403306000
11	51697070	51697071	T		11	GENIC	homozygous	403306001
11	51697082	51697083	T	C	13	GENIC	heterozygous	403306002
11	51697082	51697083	T		13	GENIC	homozygous	403306003
11	51697086	51697087	T	C	13	GENIC	homozygous	403306004
11	51697086	51697087	T		13	GENIC	heterozygous	403306005
11	51697098	51697099	T	C	14	GENIC	homozygous	138991747
11	51712576	51712577	C	T	8	GENIC	homozygous	403641089
11	51712576	51712577	C		8	GENIC	heterozygous	403641090
11	51717490	51717492	AC		15	GENIC	heterozygous	138888873