chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	53311622	53311623	T	C	15	GENIC	homozygous	51961697
9	53311732	53311734	TA	--	10	GENIC	heterozygous	52217059
9	53311841	53311842	T	-	21	GENIC	homozygous	51961698
9	53312435	53312436	G	A	21	GENIC	possibly homozygous	51961699
9	53312535	53312536	C	CG	11	GENIC	heterozygous	52394991
9	53312536	53312538	GG	--	11	GENIC	heterozygous	51961700
9	53312721	53312722	C	A	22	GENIC	homozygous	51961701
9	53313649	53313650	G	A	20	GENIC	possibly homozygous	51961702
9	53314307	53314308	C	CAAAA	12	GENIC	possibly homozygous	51961703
9	53314487	53314488	A	AGTAT	16	GENIC	homozygous	51961704
9	53314935	53314936	C	T	40	GENIC	homozygous	51961705
9	53315517	53315518	A	G	33	GENIC	homozygous	51961706