chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51391267	51391271	GTGT	----	12	GENIC	heterozygous	49947079
13	51391269	51391271	GT	--	12	GENIC	heterozygous	49947080
13	51392480	51392481	C	-	14	GENIC	homozygous	49755943
13	51392480	51392481	C	CA	15	GENIC	homozygous	49755944
13	51401652	51401653	T	TGTATGACAAA	32	GENIC	homozygous	49755993
13	51403901	51403902	T	TG	35	GENIC	homozygous	49756005
13	51403904	51403905	G	GA	28	GENIC	heterozygous	49756006
13	51407259	51407261	GT	--	18	GENIC	heterozygous	49947081
13	51409014	51409015	A	T	66	GENIC	homozygous	49756025
13	51421527	51421528	A	T	54	GENIC	possibly homozygous	49756069
13	51422086	51422087	C	CAT	19	GENIC	heterozygous	49947082
13	51422086	51422087	C	CATAT	19	GENIC	heterozygous	49947083
13	51432803	51432804	C	T	57	GENIC	homozygous	49756099
13	51449175	51449183	TCTCGCTA	--------	31	GENIC	heterozygous	49756146
13	51452999	51453000	C	-	22	GENIC	homozygous	49756154
13	51453002	51453005	ACG	---	23	GENIC	homozygous	49756155
13	51453007	51453011	CCCG	----	21	GENIC	homozygous	49756156
13	51453013	51453014	G	-	24	GENIC	homozygous	49756157