chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36481779	36481780	G	A	29	GENIC	homozygous	52040544
10	36482126	36482127	G	GT	12	GENIC	homozygous	52040546
10	36483590	36483591	T	-	18	GENIC	homozygous	51414335
10	36483591	36483592	T	A	19	GENIC	possibly homozygous	52316269
10	36485950	36485951	A	AATTG	18	GENIC	homozygous	52040548
10	36486851	36486852	A	T	26	GENIC	homozygous	51414341
10	36487693	36487694	A	-	13	GENIC	homozygous	52040552
10	36487948	36487949	G	T	29	GENIC	homozygous	51414343
10	36488259	36488260	T	C	18	GENIC	homozygous	51414345
10	36488775	36488776	C	A	11	GENIC	homozygous	51414347