chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208072899	208072900	C	T	10	GENIC	heterozygous	59357047
2	208073353	208073354	T	TCCATATACACCCTCTTG	3	GENIC	homozygous	59357048
2	208073495	208073496	C	T	19	GENIC	possibly homozygous	59357049
2	208074158	208074159	C	G	11	GENIC	homozygous	59357050
2	208074165	208074166	A	G	12	GENIC	homozygous	59357051
2	208074433	208074434	C	CAT	23	GENIC	homozygous	59357052
2	208074623	208074624	C	CA	3	GENIC	homozygous	59357053
2	208074629	208074630	T	C	5	GENIC	homozygous	59357054
2	208075011	208075012	G	C	23	GENIC	homozygous	59357055
2	208075276	208075277	G	A	4	GENIC	homozygous	59357056
2	208075282	208075283	C	T	5	GENIC	homozygous	59357057
2	208075442	208075443	T	C	6	GENIC	homozygous	59357058
2	208075455	208075456	C	T	7	GENIC	possibly homozygous	59357059
2	208076388	208076389	G	A	21	GENIC	homozygous	59357060
2	208076723	208076724	A	G	4	GENIC	homozygous	59357061
2	208076742	208076743	T	G	1	GENIC	homozygous	59357062
2	208076763	208076764	C	CCA	1	GENIC	homozygous	59357064
2	208076944	208076945	G	A	21	GENIC	homozygous	59357065
2	208077095	208077096	C	T	28	GENIC	homozygous	59357066
2	208077188	208077189	G	GGTGTCGTAA	1	GENIC	homozygous	59357067
2	208077504	208077505	G	GTC	5	GENIC	homozygous	59357068
2	208077961	208077962	A	C	7	GENIC	homozygous	59357069
2	208078079	208078080	T	C	15	GENIC	possibly homozygous	59357070
2	208078159	208078160	A	G	17	GENIC	homozygous	59357071
2	208078390	208078391	T	G	20	GENIC	homozygous	59357072
2	208078484	208078485	A	C	7	GENIC	homozygous	59357073
2	208078599	208078600	C	T	14	GENIC	possibly homozygous	59357074
2	208078953	208078954	T	C	8	GENIC	heterozygous	59357075
2	208079540	208079541	T	TC	5	GENIC	homozygous	59357076
2	208079944	208079945	G	A	18	GENIC	possibly homozygous	59357078
2	208080102	208080103	G	A	27	GENIC	homozygous	59357079
2	208080735	208080736	T	C	8	GENIC	heterozygous	59357080