chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	89597972	89597974	TC		53	GENIC	homozygous	141783682
6	89598662	89598663	C	T	57	GENIC	homozygous	141845901
6	89599605	89599611	TATTAC		55	GENIC	homozygous	141783683
6	89599688	89599689	A	G	59	GENIC	homozygous	137842040
6	89600027	89600028	C	A	55	GENIC	homozygous	141845902
6	89600280	89600281	T	G	65	GENIC	homozygous	141845903
6	89600530	89600531	C	T	24	GENIC	homozygous	141845904
6	89601312	89601312		G	69	GENIC	homozygous	141783684
6	89601780	89601781	A	G	57	GENIC	homozygous	137842046
6	89601095	89601096	T	A	48	GENIC	homozygous	137842041
6	89601111	89601112	G	A	46	GENIC	homozygous	137842042
6	89601743	89601744	C	G	59	GENIC	homozygous	137842045
6	89599565	89599567	AT		53	GENIC	homozygous	137696075
6	89603660	89603682	TCTGTGACTCTTGTTTTAGAGG		59	GENIC	homozygous	141783685
6	89604811	89604812	G	A	54	GENIC	homozygous	137842058
6	89604817	89604818	T	A	53	GENIC	homozygous	141845905
6	89604818	89604819	A	G	54	GENIC	homozygous	141845906
6	89605291	89605292	T	G	60	GENIC	homozygous	137842062
6	89605920	89605921	T	C	39	GENIC	homozygous	137842063
6	89606341	89606345	ACTC		58	GENIC	possibly homozygous	141783686
6	89606542	89606543	T	C	54	GENIC	homozygous	141845907
6	89606781	89606782	G	A	60	GENIC	homozygous	141845908
6	89606879	89606880	A	G	64	GENIC	homozygous	137842069
6	89606984	89606985	T	G	65	GENIC	possibly homozygous	137842070
6	89607642	89607643	C	A	62	GENIC	homozygous	141845909
6	89607877	89607878	C	A	51	GENIC	homozygous	141845910
6	89608102	89608103	A		67	GENIC	homozygous	137696081
6	89608131	89608132	T	C	67	GENIC	homozygous	141845911
6	89611357	89611358	G	A	49	GENIC	homozygous	141845912
6	89600530	89600531	C		24	GENIC	heterozygous	403823733