chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	65481870	65481876	TGTGTG	------	10	GENIC	homozygous	51477789
10	65483005	65483006	C	A	38	GENIC	homozygous	51477790
10	65483230	65483232	GT	--	21	GENIC	possibly homozygous	51477791
10	65483231	65483243	TGAGGCCGAGAT	------------	24	GENIC	homozygous	51477792
10	65483234	65483238	GGCC	----	18	GENIC	homozygous	51477793
10	65483235	65483243	GCCGAGAT	--------	17	GENIC	homozygous	51477794
10	65483949	65483950	T	TACAC	15	GENIC	possibly homozygous	51477795
10	65484460	65484461	C	CGAAA	23	GENIC	homozygous	51477796
10	65485198	65485202	TGTG	----	30	GENIC	heterozygous	51477797
10	65485200	65485202	TG	--	30	GENIC	possibly homozygous	51477798
10	65485711	65485712	A	G	56	GENIC	heterozygous	51477799
10	65486680	65486681	A	T	51	GENIC	homozygous	51477800
10	65487560	65487562	TC	--	16	GENIC	possibly homozygous	51477801
10	65487569	65487570	C	G	20	GENIC	possibly homozygous	51477802
10	65487577	65487578	C	G	21	GENIC	heterozygous	51477803
10	65487580	65487586	TGTGTC	------	12	GENIC	heterozygous	51477804
10	65487758	65487759	T	G	49	GENIC	possibly homozygous	51477805
10	65488034	65488038	TGTG	----	38	GENIC	heterozygous	51477806
10	65488036	65488038	TG	--	38	GENIC	possibly homozygous	51477807
10	65488321	65488323	TT	--	17	GENIC	homozygous	51477808
10	65488488	65488489	T	-	39	GENIC	homozygous	51477809