chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59839909	59839910	T	C	18	GENIC	homozygous	116608884
10	59840393	59840394	A	G	30	GENIC	homozygous	116608886
10	59840509	59840510	T	G	51	GENIC	homozygous	116608888
10	59840893	59840894	C	T	64	GENIC	homozygous	116608890
10	59842670	59842671	T	C	39	GENIC	homozygous	116608892
10	59842923	59842924	A	G	56	GENIC	homozygous	116608896
10	59843956	59843957	T	C	36	GENIC	homozygous	116608898
10	59845232	59845233	T	C	36	GENIC	possibly homozygous	117995663
10	59845669	59845670	T	C	51	GENIC	homozygous	116608900
10	59847876	59847877	C	T	35	GENIC	possibly homozygous	116608902
10	59848444	59848445	C	T	49	GENIC	homozygous	116608904
10	59850533	59850534	T	C	46	GENIC	homozygous	116608906
10	59854673	59854674	T	C	61	GENIC	homozygous	116608908
10	59860050	59860051	G	T	73	GENIC	homozygous	116608910
10	59867271	59867272	C	T	40	GENIC	homozygous	116608912
10	59872807	59872808	T	C	43	GENIC	homozygous	116608914
10	59873863	59873864	T	C	41	GENIC	homozygous	116608916
10	59874050	59874051	A	G	53	GENIC	homozygous	116608918
10	59878620	59878621	T	C	17	GENIC	homozygous	116608920
10	59886787	59886788	T	C	16	GENIC	homozygous	116608922