chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	32295683	32295684	T	A	20	GENIC	homozygous	47380330
16	32295691	32295692	A	T	22	GENIC	homozygous	47380332
16	32295700	32295701	A	-	18	GENIC	homozygous	47380334
16	32295701	32295702	T	C	18	GENIC	homozygous	47926950
16	32295706	32295707	T	A	20	GENIC	homozygous	47926951
16	32295713	32295714	T	A	20	GENIC	homozygous	47380338
16	32295715	32295716	G	C	20	GENIC	homozygous	47380340
16	32295718	32295719	T	C	23	GENIC	homozygous	47380342
16	32296112	32296113	G	GTGCTTGCTAGGCA	4	GENIC	homozygous	47926952
16	32296116	32296117	G	GCTCTACCACTGAGCTAA	2	GENIC	homozygous	47926953
16	32296121	32296122	T	C	2	GENIC	homozygous	47926954
16	32304456	32304457	G	GT	4	GENIC	heterozygous	47753606
16	32304457	32304458	T	-	4	GENIC	heterozygous	47639643
16	32313785	32313786	C	CTT	4	GENIC	heterozygous	47926955
16	32317822	32317824	TA	--	10	GENIC	heterozygous	47639652
16	32326864	32326865	G	-	8	GENIC	homozygous	47926957
16	32332760	32332764	TCTC	----	4	GENIC	heterozygous	47926958
16	32332762	32332764	TC	--	4	GENIC	heterozygous	47926959
16	32338677	32338679	CC	--	10	GENIC	heterozygous	47380357
16	32343584	32343585	T	TG	3	GENIC	homozygous	47380359
16	32343877	32343878	A	-	13	GENIC	heterozygous	47380361