chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105568558	105568559	C	CT	20	GENIC	homozygous	52084536
10	105568603	105568604	G	A	25	GENIC	homozygous	52084538
10	105569697	105569698	A	C	31	GENIC	homozygous	51761867
10	105570450	105570451	G	GGT	32	GENIC	homozygous	51761871
10	105570888	105570889	T	A	55	GENIC	homozygous	51761875
10	105570890	105570891	A	G	54	GENIC	homozygous	51761877
10	105571459	105571463	ATCC	----	3	GENIC	heterozygous	51761883
10	105571466	105571467	C	T	21	GENIC	heterozygous	51761885
10	105571474	105571475	C	T	18	GENIC	heterozygous	52084540
10	105571640	105571641	T	C	32	GENIC	homozygous	51761887
10	105571799	105571800	G	A	31	GENIC	homozygous	51761889
10	105571934	105571935	G	A	21	GENIC	homozygous	51761891
10	105572253	105572254	A	-	15	GENIC	homozygous	51761893
10	105572278	105572279	T	TA	19	GENIC	homozygous	52084542
10	105572284	105572285	T	G	21	GENIC	homozygous	52084544