chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21365128	21365129	G	C	46	GENIC	homozygous	111754517
16	21365680	21365681	T	C	45	GENIC	homozygous	111754519
16	21368152	21368153	A	T	42	GENIC	homozygous	111754521
16	21370401	21370402	A	C	51	GENIC	homozygous	111754523
16	21370482	21370483	A	G	39	GENIC	homozygous	111754525
16	21371001	21371002	A	G	42	GENIC	homozygous	111754527
16	21371048	21371049	C	T	36	GENIC	homozygous	111754529
16	21371279	21371280	A	G	42	GENIC	homozygous	111754531
16	21371325	21371326	A	G	44	GENIC	homozygous	111754533
16	21372383	21372384	G	T	52	GENIC	homozygous	111754535
16	21373897	21373898	G	A	57	GENIC	homozygous	111754537
16	21374333	21374334	A	T	21	GENIC	homozygous	111754539
16	21374343	21374344	A	G	23	GENIC	homozygous	111754541
16	21374614	21374615	G	A	46	GENIC	homozygous	111754543
16	21375093	21375094	C	T	38	GENIC	homozygous	111754545
16	21375326	21375327	C	T	47	GENIC	homozygous	111754547
16	21376129	21376130	C	G	40	GENIC	homozygous	111754549
16	21376958	21376959	T	C	43	GENIC	homozygous	111754551
16	21378319	21378320	C	T	44	GENIC	homozygous	111754553
16	21378695	21378696	C	T	42	GENIC	homozygous	111754555
16	21378696	21378697	T	C	40	GENIC	homozygous	111754557
16	21378974	21378975	G	A	36	GENIC	homozygous	111754559