chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59839909	59839910	T	C	14	GENIC	homozygous	116608884
10	59840393	59840394	A	G	19	GENIC	homozygous	116608886
10	59840509	59840510	T	G	15	GENIC	homozygous	116608888
10	59840893	59840894	C	T	24	GENIC	homozygous	116608890
10	59842670	59842671	T	C	23	GENIC	homozygous	116608892
10	59842923	59842924	A	G	25	GENIC	homozygous	116608896
10	59843439	59843439		A	21	GENIC	homozygous	128820938
10	59843956	59843957	T	C	14	GENIC	homozygous	116608898
10	59845448	59845449	A		20	GENIC	homozygous	128820940
10	59845669	59845670	T	C	24	GENIC	homozygous	116608900
10	59847876	59847877	C	T	17	GENIC	homozygous	116608902
10	59848444	59848445	C	T	17	GENIC	homozygous	116608904
10	59850533	59850534	T	C	26	GENIC	homozygous	116608906
10	59852059	59852066	GGCATTT		16	GENIC	homozygous	128820941
10	59854673	59854674	T	C	22	GENIC	homozygous	116608908
10	59860050	59860051	G	T	19	GENIC	possibly homozygous	116608910
10	59860894	59860895	G		19	GENIC	homozygous	128820943
10	59867271	59867272	C	T	19	GENIC	homozygous	116608912
10	59872807	59872808	T	C	17	GENIC	homozygous	116608914
10	59873863	59873864	T	C	20	GENIC	homozygous	116608916
10	59874050	59874051	A	G	13	GENIC	homozygous	116608918
10	59878620	59878621	T	C	11	GENIC	homozygous	116608920
10	59879928	59879928		T	19	GENIC	homozygous	128820945
10	59881052	59881053	G		18	GENIC	homozygous	128820946
10	59881189	59881189		C	23	GENIC	homozygous	128820947
10	59884139	59884139		A	9	GENIC	homozygous	128820948
10	59886787	59886788	T	C	13	GENIC	homozygous	116608922