chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	33924967	33924968	T	C	23	GENIC	possibly homozygous	54343549
6	33925636	33925637	C	T	30	GENIC	possibly homozygous	54343554
6	33925663	33925664	A	ATGT	32	GENIC	possibly homozygous	54343557
6	33925955	33925956	A	G	32	GENIC	possibly homozygous	54343560
6	33926296	33926297	T	G	26	GENIC	possibly homozygous	54343563
6	33926309	33926312	TTG	---	20	GENIC	homozygous	54343566
6	33926780	33926781	T	A	37	GENIC	homozygous	54343569
6	33927030	33927034	ACAC	----	17	GENIC	homozygous	54343572
6	33927491	33927492	G	GTT	33	GENIC	homozygous	54343575
6	33927846	33927850	CACT	----	32	GENIC	possibly homozygous	54343578
6	33927973	33927974	A	-	32	GENIC	possibly homozygous	54343581
6	33929895	33929896	C	T	28	GENIC	possibly homozygous	54343584
6	33929963	33929964	A	G	33	GENIC	possibly homozygous	54343587
6	33930183	33930184	C	T	22	GENIC	possibly homozygous	54343590
6	33930294	33930295	C	G	28	GENIC	possibly homozygous	54343593
6	33930617	33930622	TTTTG	-----	24	GENIC	homozygous	54343596
6	33933107	33933108	A	G	28	GENIC	homozygous	54343599