chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51219054	51219055	A	T	18	GENIC	possibly homozygous	114720388
13	51219218	51219219	A	C	40	GENIC	homozygous	114342877
13	51219361	51219362	G	A	26	GENIC	homozygous	114672302
13	51219822	51219823	T	A	56	GENIC	homozygous	114342879
13	51220873	51220874	A	G	52	GENIC	possibly homozygous	114342881
13	51220920	51220921	C	T	59	GENIC	possibly homozygous	114342883
13	51221355	51221356	T	C	38	GENIC	homozygous	114342885
13	51221892	51221893	T	C	42	GENIC	homozygous	114342887
13	51222356	51222357	C	T	40	GENIC	homozygous	114342889
13	51222830	51222831	T	C	58	GENIC	homozygous	114342891
13	51222946	51222947	T	C	43	GENIC	homozygous	114342893
13	51223047	51223048	T	A	63	GENIC	possibly homozygous	114342895
13	51223739	51223740	C	A	26	GENIC	homozygous	114342897
13	51224307	51224308	C	T	27	GENIC	homozygous	114342899