chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20415318	20415319	C	T	59	GENIC	homozygous	47327670
16	20416034	20416035	T	C	63	GENIC	possibly homozygous	47327672
16	20416039	20416040	G	A	63	GENIC	possibly homozygous	47327674
16	20416198	20416199	G	GTT	15	GENIC	possibly homozygous	47327676
16	20416812	20416824	TCTCTCTCTCTC	------------	4	GENIC	homozygous	47327678
16	20416860	20416861	T	A	24	GENIC	heterozygous	47627368
16	20417475	20417476	G	A	50	GENIC	homozygous	47327680
16	20418883	20418884	G	A	53	GENIC	homozygous	47327682
16	20419092	20419093	A	C	75	GENIC	homozygous	47327684
16	20419272	20419274	AA	--	27	GENIC	homozygous	47327686
16	20419303	20419304	T	TAA	27	GENIC	heterozygous	47327688
16	20419303	20419304	T	TA	27	GENIC	heterozygous	47327690
16	20419304	20419305	A	AT	40	GENIC	possibly homozygous	47327692
16	20419305	20419306	A	T	47	GENIC	heterozygous	47627370
16	20419821	20419822	G	A	54	INTERGENIC	homozygous	47327694
16	20422834	20422835	G	T	55	INTERGENIC	homozygous	47327696