chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	121155928	121155929	G	GTTT	23	GENIC	possibly homozygous	52311403
9	121155928	121155929	G	GTT	23	GENIC	heterozygous	53058305
9	121155954	121155955	T	-	28	GENIC	possibly homozygous	52311404
9	121155988	121155989	A	T	27	GENIC	homozygous	53349283
9	121158838	121158842	ACGT	----	15	GENIC	homozygous	52311405
9	121158890	121158891	T	C	16	GENIC	homozygous	52156840
9	121160081	121160082	T	A	17	GENIC	homozygous	52156842
9	121160475	121160476	G	A	16	GENIC	homozygous	52311406
9	121162078	121162079	A	AAC	1	GENIC	homozygous	52156844
9	121165895	121165896	T	C	20	GENIC	homozygous	52311407
9	121173502	121173503	A	G	22	GENIC	homozygous	52156852
9	121174033	121174034	C	CAAG	28	GENIC	homozygous	52156854