chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41489650	41489651	G	A	3	GENIC	homozygous	117006197
10	41490466	41490467	A	C	4	GENIC	homozygous	117409936
10	41490624	41490625	G	T	14	GENIC	heterozygous	117409938
10	41490646	41490647	G	A	15	GENIC	heterozygous	117409940
10	41490661	41490662	G	A	14	GENIC	homozygous	117409942
10	41490663	41490664	A	C	13	GENIC	heterozygous	117409944
10	41490664	41490665	G	A	12	GENIC	heterozygous	117409946
10	41490672	41490673	A	C	12	GENIC	homozygous	117006201
10	41490680	41490681	T	C	11	GENIC	homozygous	117409948
10	41490700	41490701	G	T	10	GENIC	heterozygous	117409950
10	41490701	41490702	C	A	9	GENIC	heterozygous	117409952
10	41490711	41490712	T	A	2	GENIC	homozygous	117006203
10	41490726	41490727	G	C	2	GENIC	homozygous	117006205
10	41490881	41490882	A	G	7	GENIC	homozygous	116571815
10	41491162	41491163	C	G	5	GENIC	homozygous	116571817
10	41491414	41491415	A	G	2	GENIC	homozygous	117409954
10	41491420	41491421	G	A	2	GENIC	homozygous	117409956
10	41491430	41491431	T	G	2	GENIC	homozygous	117409958
10	41491511	41491512	A	T	4	GENIC	heterozygous	117409960