chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	80643630	80643631	G	C	7	GENIC	heterozygous	47562839
16	80645033	80645034	G	A	43	GENIC	homozygous	47562843
16	80649019	80649020	G	T	28	GENIC	possibly homozygous	47562845
16	80649153	80649154	G	T	42	GENIC	homozygous	47562847
16	80651590	80651591	G	-	17	GENIC	possibly homozygous	47562849
16	80651669	80651670	G	A	28	GENIC	possibly homozygous	47562851
16	80651992	80651993	C	T	50	GENIC	possibly homozygous	47562853
16	80652536	80652537	C	T	35	GENIC	homozygous	47562855
16	80654736	80654737	T	C	34	GENIC	homozygous	47562857
16	80654857	80654858	T	C	41	GENIC	homozygous	47562859
16	80655160	80655161	G	A	36	GENIC	homozygous	47562861
16	80655863	80655864	C	T	36	GENIC	homozygous	47562863
16	80656781	80656782	A	G	32	GENIC	homozygous	47562865
16	80657048	80657049	T	TC	21	GENIC	heterozygous	47562867
16	80657049	80657050	T	C	23	GENIC	heterozygous	47562869
16	80657049	80657050	T	TCTC	21	GENIC	possibly homozygous	47562871
16	80657078	80657079	A	G	22	GENIC	homozygous	47562873
16	80657302	80657303	T	C	26	GENIC	homozygous	47562875
16	80657402	80657403	T	C	28	GENIC	homozygous	47562877
16	80657577	80657578	T	C	27	GENIC	homozygous	47562879
16	80657683	80657684	T	C	27	GENIC	homozygous	47562881