chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	41017578	41017579	T	C	36	GENIC	homozygous	51926773
9	41017790	41017791	A	G	21	GENIC	homozygous	51926775
9	41017867	41017868	T	C	19	GENIC	homozygous	51926779
9	41018150	41018151	A	G	36	GENIC	homozygous	51926783
9	41021366	41021367	G	GTT	19	GENIC	homozygous	52381253
9	41021374	41021376	GG	--	19	GENIC	heterozygous	51926807
9	41023558	41023559	C	A	49	GENIC	possibly homozygous	52381255
9	41027136	41027137	A	AGT	17	GENIC	heterozygous	51926841
9	41027622	41027624	TG	--	19	GENIC	heterozygous	52381261
9	41027664	41027665	A	ATGTG	16	GENIC	homozygous	51926856
9	41027987	41027988	A	G	34	GENIC	homozygous	51926863
9	41030173	41030175	TG	--	14	GENIC	homozygous	52381265
9	41032764	41032765	T	G	29	GENIC	heterozygous	51926901
9	41033573	41033575	TG	--	10	GENIC	heterozygous	52381267
9	41034496	41034498	TG	--	18	GENIC	homozygous	51926915
9	41037733	41037734	G	-	24	GENIC	heterozygous	51926933
9	41043215	41043217	AT	--	32	GENIC	possibly homozygous	52381275
9	41030353	41030354	A	AGT	7	GENIC	heterozygous	52543075