chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	42485906	42485907	T	C	31	GENIC	homozygous	52178969
9	42486100	42486101	C	A	33	GENIC	homozygous	52178971
9	42486483	42486484	C	T	41	GENIC	homozygous	52385822
9	42486555	42486556	C	A	29	GENIC	homozygous	52178972
9	42486703	42486704	A	G	29	GENIC	homozygous	52178973
9	42487209	42487210	G	A	24	GENIC	homozygous	52178974
9	42487262	42487263	A	G	37	GENIC	homozygous	52178975
9	42487514	42487516	TT	--	42	GENIC	possibly homozygous	52178976
9	42487877	42487878	G	A	22	GENIC	homozygous	52385824
9	42487996	42488000	TGTG	----	30	GENIC	possibly homozygous	52385826
9	42489365	42489366	T	-	29	GENIC	homozygous	52178979
9	42490401	42490402	C	T	33	GENIC	homozygous	52178980
9	42492097	42492098	T	C	33	GENIC	homozygous	52178982
9	42492314	42492315	A	G	31	GENIC	homozygous	52178983
9	42492521	42492522	T	G	26	GENIC	homozygous	52178984
9	42492846	42492850	TCTC	----	13	GENIC	heterozygous	53190486
9	42492864	42492865	T	G	11	GENIC	possibly homozygous	52178985
9	42492876	42492877	G	GCACACACACACACA	7	GENIC	heterozygous	53352456
9	42492938	42492939	C	T	22	GENIC	homozygous	52385830
9	42493353	42493354	C	G	46	GENIC	homozygous	52178986
9	42492876	42492877	G	GCACACACACA	7	GENIC	possibly homozygous	53572457