chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	21226938	21226939	C	CGT	2	GENIC	homozygous	50108483
12	21231178	21231179	G	GCT	4	GENIC	homozygous	50108489
12	21231330	21231331	G	C	19	GENIC	homozygous	50108491
12	21231331	21231332	G	T	18	GENIC	homozygous	50108493
12	21231332	21231333	G	T	18	GENIC	homozygous	50108495
12	21232938	21232939	C	CTG	17	GENIC	possibly homozygous	50108519
12	21232456	21232457	A	AGAAAGAAAGAAAGAAAGAAG	5	GENIC	homozygous	50537620
12	21232918	21232919	C	CTCTGTGTGTGTGCGTGGGTGTGGGTG	22	GENIC	homozygous	50537622
12	21234166	21234170	ATAC	----	5	GENIC	homozygous	50537624
12	21234586	21234587	T	TGG	3	GENIC	homozygous	50537626
12	21234365	21234366	C	G	7	GENIC	homozygous	50108545