chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59829761	59829762	T	C	21	GENIC	homozygous	116608848
10	59830008	59830009	C	T	26	GENIC	homozygous	116608850
10	59830162	59830163	G	A	7	GENIC	homozygous	116608852
10	59830384	59830385	C	T	24	GENIC	homozygous	116608854
10	59830934	59830935	T	C	26	GENIC	homozygous	116608856
10	59831668	59831669	G	C	17	GENIC	homozygous	116608858
10	59831748	59831749	G	A	23	GENIC	homozygous	116608860
10	59831819	59831820	C	A	21	GENIC	homozygous	116608862
10	59831972	59831973	C	T	24	GENIC	homozygous	116608864
10	59832312	59832313	T	C	24	GENIC	homozygous	116608866
10	59832674	59832675	G	A	30	GENIC	homozygous	116608868
10	59832857	59832858	G	T	14	GENIC	homozygous	116608870
10	59832926	59832927	T	C	17	GENIC	homozygous	116608872
10	59833087	59833088	C	T	17	GENIC	homozygous	116608874
10	59834399	59834400	G	T	22	GENIC	homozygous	116608876
10	59834851	59834852	A	T	14	GENIC	homozygous	116608878
10	59837293	59837294	G	A	9	GENIC	homozygous	116608880
10	59837916	59837917	A	G	10	GENIC	homozygous	116608882
10	59839909	59839910	T	C	12	GENIC	homozygous	116608884
10	59840393	59840394	A	G	13	GENIC	homozygous	116608886
10	59840509	59840510	T	G	15	GENIC	heterozygous	116608888
10	59840893	59840894	C	T	19	GENIC	homozygous	116608890
10	59842923	59842924	A	G	23	GENIC	homozygous	116608896
10	59843956	59843957	T	C	13	GENIC	homozygous	116608898
10	59845232	59845233	T	C	8	GENIC	heterozygous	117995663
10	59845669	59845670	T	C	16	GENIC	homozygous	116608900
10	59847876	59847877	C	T	16	GENIC	homozygous	116608902
10	59848444	59848445	C	T	14	GENIC	homozygous	116608904
10	59850533	59850534	T	C	8	GENIC	homozygous	116608906
10	59852064	59852065	T	A	5	GENIC	heterozygous	126383385
10	59852065	59852066	T	A	4	GENIC	heterozygous	126383386
10	59854673	59854674	T	C	30	GENIC	homozygous	116608908
10	59860050	59860051	G	T	26	GENIC	homozygous	116608910