chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66053903	66053904	T	-	7	GENIC	heterozygous	52440870
10	66057036	66057037	A	-	9	GENIC	heterozygous	52382533
10	66058607	66058608	C	-	16	GENIC	heterozygous	51479039
10	66058607	66058608	C	T	15	GENIC	heterozygous	52382535
10	66060082	66060083	G	GA	2	GENIC	heterozygous	51479041
10	66060083	66060084	A	-	2	GENIC	heterozygous	51479042
10	66062847	66062848	T	C	25	GENIC	homozygous	51479043
10	66063021	66063022	C	CA	7	GENIC	heterozygous	51479045
10	66065419	66065420	C	CTTTT	15	GENIC	homozygous	51479049
10	66066178	66066179	T	TCTTCTGGAGTGTCTGAAGACAGTGACAGTGTAGTG	5	GENIC	homozygous	52382537
10	66066190	66066191	A	ACACACATTAAATAAATAAATAAATTTTTTTATTTAATGTGTGCGAGTACAAAGTCACT	4	GENIC	homozygous	52382539
10	66066391	66066392	G	C	11	GENIC	homozygous	51479050
10	66068623	66068624	T	G	14	GENIC	homozygous	51479055
10	66068674	66068675	T	-	5	GENIC	heterozygous	52440874
10	66068967	66068968	A	AT	6	GENIC	heterozygous	51479056
10	66068967	66068968	A	ATT	6	GENIC	heterozygous	52724620
10	66069835	66069836	A	-	2	GENIC	homozygous	51479058
10	66071482	66071483	A	AACAC	5	GENIC	homozygous	51479060
10	66076016	66076017	G	GAA	13	GENIC	possibly homozygous	51479068
10	66076016	66076017	G	GAAA	13	GENIC	heterozygous	51479069
10	66078256	66078257	A	ATG	19	GENIC	heterozygous	51907726
10	66066141	66066142	G	T	13	GENIC	homozygous	51907720
10	66069821	66069822	C	T	12	GENIC	homozygous	51907722
10	66076715	66076716	C	CTGTTTGTT	10	GENIC	homozygous	51907724
10	66078256	66078257	A	ATGTG	19	GENIC	heterozygous	52159203
10	66081508	66081509	C	T	12	GENIC	homozygous	51907730