chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13411296	13411297	T	A	22	GENIC	homozygous	116735792
10	13411833	13411834	G	A	28	GENIC	homozygous	116495986
10	13412715	13412716	G	A	23	GENIC	homozygous	116735793
10	13412999	13413000	T	C	22	GENIC	homozygous	116495988
10	13413527	13413528	C	A	31	GENIC	homozygous	116495990
10	13413612	13413613	G	C	26	GENIC	homozygous	116495992
10	13413771	13413772	A	G	34	GENIC	homozygous	116495994
10	13413856	13413857	C	T	33	GENIC	homozygous	116735794
10	13413934	13413935	G	A	35	GENIC	homozygous	116735795
10	13413984	13413985	T	C	30	GENIC	homozygous	116495996
10	13414021	13414022	G	A	30	GENIC	homozygous	116496000
10	13414048	13414049	T	C	22	GENIC	homozygous	116496002
10	13414061	13414062	C	T	22	GENIC	homozygous	116496004
10	13414086	13414087	C	T	25	GENIC	homozygous	116496006
10	13414103	13414104	T	C	25	GENIC	homozygous	116496008
10	13414302	13414303	G	A	25	GENIC	homozygous	116735796
10	13415429	13415430	C	T	28	GENIC	homozygous	116735797
10	13415811	13415812	C	T	25	GENIC	homozygous	116735798
10	13415812	13415813	A	G	25	GENIC	homozygous	116496012
10	13416132	13416133	C	T	20	GENIC	homozygous	116735799
10	13417451	13417452	G	A	26	GENIC	homozygous	116496016