chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	212589681	212589682	T	C	42	GENIC	possibly homozygous	108988522
1	212589772	212589773	C	T	61	GENIC	homozygous	108988523
1	212589960	212589961	T	C	55	GENIC	homozygous	108988524
1	212589999	212590000	T	C	63	GENIC	homozygous	108988526
1	212591315	212591316	A	T	37	GENIC	homozygous	120591659
1	212591388	212591389	G	A	32	GENIC	homozygous	120591662
1	212591669	212591670	C	T	44	GENIC	homozygous	108988535
1	212591999	212592000	C	T	26	GENIC	homozygous	120591664
1	212592258	212592259	T	C	29	GENIC	homozygous	108988540
1	212593662	212593663	T	G	36	GENIC	homozygous	108988554
1	212597126	212597127	A	G	29	GENIC	homozygous	108988591
1	212598085	212598086	G	A	33	GENIC	homozygous	120591666
1	212598279	212598280	C	T	24	GENIC	homozygous	120591668
1	212601182	212601183	A	G	36	GENIC	homozygous	108988606
1	212601986	212601987	C	T	53	GENIC	homozygous	120591670
1	212602821	212602822	T	G	27	GENIC	homozygous	108988609