chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	53311622	53311623	T	C	17	GENIC	homozygous	51961697
9	53311733	53311734	A	G	21	GENIC	possibly homozygous	52854668
9	53311841	53311842	T	-	19	GENIC	homozygous	51961698
9	53312435	53312436	G	A	20	GENIC	homozygous	51961699
9	53312721	53312722	C	A	30	GENIC	possibly homozygous	51961701
9	53313649	53313650	G	A	30	GENIC	homozygous	51961702
9	53314307	53314308	C	CAAAA	7	GENIC	possibly homozygous	51961703
9	53314307	53314308	C	CAAA	7	GENIC	heterozygous	52907278
9	53314487	53314488	A	AGTAT	18	GENIC	homozygous	51961704
9	53314935	53314936	C	T	35	GENIC	homozygous	51961705
9	53315517	53315518	A	G	28	GENIC	homozygous	51961706