chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	214180001	214180003	TT	--	23	GENIC	possibly homozygous	61318967
1	214180025	214180026	A	C	34	GENIC	homozygous	61079796
1	214180082	214180083	C	G	38	GENIC	homozygous	61079797
1	214180539	214180540	C	A	31	GENIC	homozygous	61079798
1	214180752	214180753	C	T	39	GENIC	homozygous	61079799
1	214181151	214181152	T	-	32	GENIC	homozygous	61079800
1	214181330	214181331	A	G	18	GENIC	homozygous	61079801
1	214181334	214181335	A	G	17	GENIC	homozygous	61079802
1	214181346	214181347	G	T	18	GENIC	homozygous	61079803
1	214181349	214181350	G	T	17	GENIC	homozygous	61079804
1	214181352	214181353	A	T	17	GENIC	homozygous	61079805
1	214181357	214181358	A	T	17	GENIC	homozygous	61079806
1	214181360	214181361	A	G	19	GENIC	homozygous	61079807
1	214181361	214181362	A	G	19	GENIC	homozygous	61079808
1	214181363	214181364	A	G	19	GENIC	homozygous	61079809
1	214181391	214181392	A	G	24	GENIC	homozygous	61079810
1	214181548	214181549	C	T	27	GENIC	homozygous	61079811
1	214181596	214181597	C	-	21	GENIC	homozygous	61079812
1	214181752	214181753	T	C	30	GENIC	homozygous	61079813