chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	203984033	203984034	G	A	10	GENIC	homozygous	61584653
1	203985006	203985007	G	A	9	GENIC	homozygous	61061110
1	203985901	203985902	G	A	19	GENIC	possibly homozygous	61584654
1	203985939	203985940	A	G	19	GENIC	homozygous	61061113
1	203986413	203986414	C	T	11	GENIC	homozygous	61584655
1	203986421	203986422	A	T	13	GENIC	homozygous	61061115
1	203986486	203986487	A	T	17	GENIC	homozygous	61061116
1	203987362	203987363	C	T	17	GENIC	possibly homozygous	61584658
1	203987427	203987428	T	TGG	3	GENIC	heterozygous	61061117
1	203988584	203988585	A	-	9	GENIC	possibly homozygous	61061120
1	203988997	203988998	T	C	7	GENIC	heterozygous	61061121
1	203989090	203989091	G	A	8	GENIC	possibly homozygous	61061122
1	203989319	203989320	G	T	9	GENIC	possibly homozygous	61061124
1	203990385	203990386	A	G	19	GENIC	homozygous	61061132
1	203990500	203990501	A	AT	5	GENIC	homozygous	61584659
1	203990662	203990663	T	C	20	GENIC	homozygous	61061133
1	203990852	203990853	G	T	15	GENIC	possibly homozygous	61061134
1	203990969	203990970	T	G	13	GENIC	possibly homozygous	61584660
1	203996907	203996908	A	G	10	GENIC	possibly homozygous	61061147
1	203999511	203999512	A	G	2	GENIC	homozygous	61061151
1	204000939	204000940	C	T	26	GENIC	homozygous	61584665
1	204003297	204003298	T	C	6	GENIC	heterozygous	61061157
1	204005989	204005990	T	C	8	GENIC	heterozygous	61584666
1	204006610	204006611	C	G	18	GENIC	possibly homozygous	61061161
1	204007005	204007006	A	G	15	GENIC	homozygous	61061162