chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66053900	66053901	A	AT	12	GENIC	heterozygous	52382531
10	66058607	66058608	C	T	17	GENIC	possibly homozygous	52382535
10	66060082	66060083	G	GA	13	GENIC	heterozygous	51479041
10	66060083	66060084	A	-	13	GENIC	heterozygous	51479042
10	66062847	66062848	T	C	22	GENIC	homozygous	51479043
10	66063021	66063022	C	CA	6	GENIC	heterozygous	51479045
10	66065419	66065420	C	CTTTT	32	GENIC	homozygous	51479049
10	66066178	66066179	T	TCTTCTGGAGTGTCTGAAGACAGTGACAGTGTAGTG	9	GENIC	homozygous	52382537
10	66066190	66066191	A	ACACACATTAAATAAATAAATAAATTTTTTTATTTAATGTGTGCGAGTACAAAGTCACT	7	GENIC	homozygous	52382539
10	66066391	66066392	G	C	29	GENIC	homozygous	51479050
10	66066514	66066515	C	CT	17	GENIC	heterozygous	52440872
10	66066824	66066825	C	CT	5	GENIC	heterozygous	51479051
10	66068623	66068624	T	G	16	GENIC	homozygous	51479055
10	66068967	66068968	A	AT	21	GENIC	possibly homozygous	51479056
10	66069306	66069314	AGAGAGGC	--------	6	GENIC	homozygous	52382541
10	66069835	66069836	A	-	7	GENIC	heterozygous	51479058
10	66071482	66071483	A	AACAC	10	GENIC	homozygous	51479060
10	66076016	66076017	G	GAA	9	GENIC	heterozygous	51479068
10	66076016	66076017	G	GAAA	9	GENIC	heterozygous	51479069
10	66076016	66076017	G	GA	9	GENIC	heterozygous	52382543
10	66078256	66078257	A	ATGTG	22	GENIC	possibly homozygous	52159203
10	66066141	66066142	G	T	12	GENIC	homozygous	51907720
10	66069821	66069822	C	T	11	GENIC	homozygous	51907722
10	66076715	66076716	C	CTGTTTGTT	17	GENIC	homozygous	51907724
10	66078256	66078257	A	ATG	22	GENIC	heterozygous	51907726
10	66081508	66081509	C	T	29	GENIC	homozygous	51907730
10	66068967	66068968	A	ATT	21	GENIC	heterozygous	52724620