chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13129167	13129168	A	G	9	GENIC	homozygous	116735648
10	13129349	13129350	T	A	12	GENIC	homozygous	116735649
10	13132115	13132116	T	A	7	GENIC	homozygous	116735651
10	13132247	13132248	G	A	18	GENIC	homozygous	116735652
10	13132739	13132740	A	G	18	GENIC	homozygous	116735653
10	13133216	13133217	T	C	16	GENIC	homozygous	116735654
10	13133802	13133803	A	G	5	GENIC	homozygous	116735655
10	13135290	13135291	C	T	18	GENIC	homozygous	116735656
10	13135543	13135544	C	T	22	GENIC	homozygous	116735657
10	13135579	13135580	A	G	19	GENIC	homozygous	116735658
10	13135596	13135597	C	T	15	GENIC	homozygous	116735659
10	13143838	13143839	A	C	26	GENIC	homozygous	116735660
10	13146777	13146778	A	C	29	GENIC	homozygous	116735661
10	13147436	13147437	C	T	21	GENIC	homozygous	116735662
10	13148885	13148886	T	C	19	GENIC	homozygous	116735663
10	13152029	13152030	T	C	14	GENIC	homozygous	116735666
10	13154798	13154799	A	G	17	GENIC	homozygous	116735667
10	13162098	13162099	A	G	14	GENIC	homozygous	116735669
10	13133933	13133934	T	C	9	GENIC	homozygous	116495623
10	13133934	13133935	C	T	9	GENIC	homozygous	116495625
10	13134137	13134138	G	T	15	GENIC	homozygous	117074870
10	13159426	13159427	C	A	10	GENIC	heterozygous	117074871