chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35498798	35498799	T	C	2	GENIC	homozygous	51407772
10	35498876	35498877	C	-	2	GENIC	heterozygous	51407774
10	35498885	35498886	A	G	2	GENIC	heterozygous	51407776
10	35499775	35499776	C	T	27	GENIC	possibly homozygous	51407780
10	35500492	35500493	G	A	9	GENIC	possibly homozygous	51407782
10	35500911	35500912	C	A	16	GENIC	heterozygous	52137743
10	35501476	35501477	C	T	5	GENIC	homozygous	51407786
10	35501934	35501935	T	C	18	GENIC	possibly homozygous	51407788
10	35502123	35502124	A	G	21	GENIC	possibly homozygous	51407790
10	35502419	35502420	A	T	21	GENIC	possibly homozygous	51407792
10	35502440	35502441	G	A	18	GENIC	homozygous	51407794
10	35502524	35502525	C	T	21	GENIC	possibly homozygous	51407796
10	35502846	35502847	G	A	20	GENIC	homozygous	51407798
10	35503402	35503403	G	T	9	GENIC	homozygous	51407800
10	35503411	35503412	G	T	11	GENIC	homozygous	51407802
10	35504021	35504022	T	C	18	GENIC	homozygous	51407804
10	35504127	35504128	A	T	2	GENIC	homozygous	51407806
10	35504160	35504161	A	G	3	GENIC	homozygous	51407808
10	35504496	35504497	A	G	5	GENIC	homozygous	51407810
10	35504688	35504689	G	C	12	GENIC	homozygous	51407812
10	35505115	35505116	T	C	21	GENIC	homozygous	51407820
10	35505362	35505363	G	A	16	GENIC	possibly homozygous	51407822
10	35505903	35505904	T	C	20	GENIC	homozygous	51407824