chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	3837008	3837009	A	T	24	GENIC	homozygous	47796816
16	3837020	3837021	C	T	24	GENIC	homozygous	47796817
16	3838723	3838724	C	T	31	GENIC	homozygous	47796818
16	3845412	3845413	G	A	30	GENIC	possibly homozygous	47796819
16	3847091	3847092	G	A	43	GENIC	homozygous	47796820
16	3847665	3847666	A	ATG	14	GENIC	possibly homozygous	47714995
16	3847690	3847691	C	T	24	GENIC	heterozygous	47796821
16	3847694	3847695	T	TGC	10	GENIC	homozygous	47796822
16	3853977	3853978	C	G	22	GENIC	homozygous	47248436
16	3860104	3860105	T	C	41	GENIC	homozygous	47796823
16	3862908	3862912	GTGT	----	1	GENIC	homozygous	47714996
16	3863661	3863662	T	A	3	GENIC	homozygous	47248437
16	3863664	3863665	T	A	3	GENIC	homozygous	47248438
16	3864766	3864770	TCTC	----	8	GENIC	homozygous	47248440
16	3867758	3867759	A	C	25	GENIC	homozygous	47248443
16	3867759	3867760	T	C	25	GENIC	homozygous	47248444
16	3867979	3867981	CA	--	20	GENIC	possibly homozygous	47796824
16	3868009	3868010	C	G	25	GENIC	heterozygous	47796825
16	3868376	3868377	G	GA	24	GENIC	possibly homozygous	47248445
16	3869061	3869066	CAGTG	-----	6	GENIC	homozygous	47796826
16	3869385	3869386	C	CTG	5	GENIC	heterozygous	47796827
16	3871764	3871765	A	ATATGTATG	36	GENIC	heterozygous	47248450
16	3871764	3871765	A	ATATG	36	GENIC	heterozygous	47796828
16	3871780	3871781	C	G	43	GENIC	heterozygous	47248451
16	3871837	3871838	T	G	21	GENIC	heterozygous	47796829
16	3871936	3871937	C	G	27	GENIC	heterozygous	47248453
16	3871940	3871941	C	G	30	GENIC	heterozygous	47796830
16	3871944	3871945	C	G	30	GENIC	heterozygous	47796831
16	3871948	3871949	C	G	33	GENIC	heterozygous	47796832
16	3871952	3871953	C	G	33	GENIC	heterozygous	47796833