chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	32295683	32295684	T	A	22	GENIC	homozygous	47380330
16	32295691	32295692	A	T	19	GENIC	homozygous	47380332
16	32295700	32295701	A	-	19	GENIC	homozygous	47380334
16	32295701	32295702	T	C	19	GENIC	homozygous	47926950
16	32295706	32295707	T	A	18	GENIC	homozygous	47926951
16	32295713	32295714	T	A	19	GENIC	homozygous	47380338
16	32295715	32295716	G	C	18	GENIC	homozygous	47380340
16	32295718	32295719	T	C	20	GENIC	homozygous	47380342
16	32296112	32296113	G	GTGCTTGCTAGGCA	3	GENIC	homozygous	47926952
16	32296116	32296117	G	GCTCTACCACTGAGCTAA	3	GENIC	homozygous	47926953
16	32296121	32296122	T	C	3	GENIC	homozygous	47926954
16	32304456	32304457	G	GT	11	GENIC	heterozygous	47753606
16	32304457	32304458	T	-	11	GENIC	heterozygous	47639643
16	32313785	32313786	C	CTT	1	GENIC	homozygous	47926955
16	32321104	32321108	TCTA	----	11	GENIC	homozygous	47926956
16	32326864	32326865	G	-	10	GENIC	homozygous	47926957
16	32332760	32332764	TCTC	----	9	GENIC	heterozygous	47926958
16	32332762	32332764	TC	--	9	GENIC	heterozygous	47926959
16	32343584	32343585	T	TG	10	GENIC	homozygous	47380359
16	32326894	32326899	CATGA	-----	13	GENIC	heterozygous	48053600
16	32333574	32333575	C	CT	13	GENIC	heterozygous	47956675