chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4733282	4733283	C	T	27	GENIC	homozygous	50005005
12	4733844	4733845	T	G	29	GENIC	homozygous	50005007
12	4736830	4736838	TTATTTAT	--------	9	GENIC	heterozygous	50395069
12	4739445	4739446	G	T	27	GENIC	homozygous	50005016
12	4739594	4739595	G	T	27	GENIC	homozygous	50005018
12	4739616	4739617	G	GCT	20	GENIC	homozygous	50005026
12	4739631	4739632	G	A	21	GENIC	homozygous	50005028
12	4739653	4739654	G	T	26	GENIC	homozygous	50005030
12	4739705	4739706	C	A	29	GENIC	homozygous	50005032
12	4739382	4739383	A	G	23	GENIC	possibly homozygous	51030670