chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109571280	109571281	G	A	26	GENIC	homozygous	116718603
10	109571355	109571356	G	C	26	GENIC	homozygous	116718605
10	109571465	109571466	C	A	27	GENIC	homozygous	116718607
10	109571570	109571571	T	A	10	GENIC	homozygous	116718609
10	109571598	109571599	T	A	3	GENIC	homozygous	116843096
10	109583690	109583691	G	A	12	GENIC	homozygous	116718619
10	109583691	109583692	A	G	11	GENIC	homozygous	116718621
10	109583698	109583699	A	C	9	GENIC	homozygous	116718623
10	109583706	109583707	G	T	8	GENIC	homozygous	116718625
10	109583710	109583711	A	G	7	GENIC	homozygous	116718627
10	109583716	109583717	A	C	7	GENIC	homozygous	116718629
10	109583725	109583726	A	C	6	GENIC	homozygous	116718631
10	109583728	109583729	T	C	4	GENIC	homozygous	116718633
10	109583729	109583730	T	A	4	GENIC	homozygous	116718635
10	109594759	109594760	A	G	27	GENIC	homozygous	116718651
10	109594955	109594956	T	G	27	GENIC	homozygous	116718655
10	109603935	109603936	T	G	17	GENIC	homozygous	116718687
10	109603936	109603937	T	G	17	GENIC	homozygous	116718689
10	109609829	109609830	A	G	9	GENIC	homozygous	116843098
10	109609936	109609937	C	G	2	GENIC	homozygous	117105495
10	109609978	109609979	C	G	3	GENIC	homozygous	117181331