chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19132221	19132222	G	A	48	GENIC	homozygous	139889660
16	19132299	19132300	C	T	52	GENIC	homozygous	139889661
16	19132571	19132572	C	T	62	GENIC	homozygous	139889662
16	19133053	19133054	T	G	60	GENIC	possibly homozygous	139889663
16	19133144	19133145	T	C	64	GENIC	homozygous	139889664
16	19133808	19133809	T	G	46	GENIC	homozygous	139889665
16	19133968	19133969	G	A	54	GENIC	homozygous	139889666
16	19135718	19135718		ATGCCCACGTCCATCCCA	33	GENIC	possibly homozygous	139824787
16	19136546	19136547	C	T	37	GENIC	homozygous	139889667
16	19136916	19136917	G	A	31	GENIC	homozygous	139889668
16	19137508	19137509	T	A	24	GENIC	homozygous	139889669
16	19138012	19138013	T		27	GENIC	homozygous	139824788
16	19140053	19140053		AA	33	GENIC	homozygous	139824789
16	19140084	19140085	A	G	42	GENIC	homozygous	139889673
16	19138142	19138143	T	C	30	GENIC	homozygous	139889670
16	19139375	19139376	A	G	31	GENIC	homozygous	139889671
16	19139708	19139709	G	A	48	GENIC	homozygous	139889672
16	19141060	19141061	T	C	38	GENIC	homozygous	139889674
16	19141768	19141769	G	A	28	GENIC	homozygous	139889675
16	19141880	19141881	A	G	47	GENIC	homozygous	139889676
16	19141956	19141957	G	A	53	GENIC	homozygous	139889677
16	19142055	19142056	T	C	44	GENIC	homozygous	139889678