chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105568635	105568636	T	C	13	GENIC	homozygous	51761865
10	105569385	105569389	TTTT	----	22	GENIC	possibly homozygous	52850660
10	105569697	105569698	A	C	37	GENIC	homozygous	51761867
10	105570450	105570451	G	GGT	17	GENIC	homozygous	51761871
10	105570845	105570846	T	A	22	GENIC	homozygous	51761873
10	105570888	105570889	T	A	24	GENIC	homozygous	51761875
10	105570890	105570891	A	G	24	GENIC	homozygous	51761877
10	105571319	105571320	C	A	38	GENIC	homozygous	51761879
10	105571458	105571459	T	TATCCATCC	12	GENIC	homozygous	53176077
10	105571640	105571641	T	C	26	GENIC	homozygous	51761887
10	105571799	105571800	G	A	21	GENIC	homozygous	51761889
10	105571934	105571935	G	A	26	GENIC	homozygous	51761891
10	105572253	105572254	A	-	22	GENIC	homozygous	51761893