chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20799456	20799457	G	T	32	GENIC	possibly homozygous	119099767
16	20799508	20799509	T	G	11	GENIC	homozygous	119099768
16	20799517	20799518	C	G	22	GENIC	possibly homozygous	119099769
16	20799525	20799526	A	T	27	GENIC	homozygous	119099770
16	20799566	20799567	T	G	24	GENIC	homozygous	119099771
16	20799578	20799579	C	A	21	GENIC	homozygous	119099772
16	20799589	20799590	C	G	16	GENIC	homozygous	119099773
16	20799595	20799596	T	G	14	GENIC	homozygous	112320126
16	20799598	20799599	A	G	13	GENIC	homozygous	119099774
16	20799608	20799609	C	T	12	GENIC	homozygous	119099775
16	20799617	20799618	C	A	6	GENIC	homozygous	119099776
16	20799903	20799904	T	C	44	GENIC	homozygous	111948911
16	20800393	20800394	T	A	44	GENIC	homozygous	111753551
16	20800933	20800934	C	G	31	GENIC	homozygous	111753553
16	20801463	20801464	C	G	53	GENIC	homozygous	111753555
16	20801662	20801663	T	C	51	GENIC	possibly homozygous	111753557
16	20804190	20804191	G	A	24	GENIC	homozygous	111753559
16	20806173	20806174	T	A	34	GENIC	homozygous	111753561
16	20806276	20806277	G	A	56	GENIC	homozygous	111753563
16	20806332	20806333	T	C	60	GENIC	homozygous	111753565
16	20806625	20806626	C	T	62	GENIC	possibly homozygous	111753567