chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47562140	47562141	C	T	39	GENIC	homozygous	115344362
12	47567928	47567929	T	C	35	GENIC	homozygous	115511951
12	47569468	47569469	T	C	26	GENIC	homozygous	115344376
12	47569486	47569487	A	T	27	GENIC	homozygous	115511952
12	47570569	47570570	T	C	28	GENIC	homozygous	115344380
12	47573733	47573734	T	A	30	GENIC	homozygous	115511953
12	47577198	47577199	T	C	39	GENIC	homozygous	115344406
12	47580546	47580547	C	T	35	GENIC	homozygous	115397669
12	47580906	47580907	C	T	49	GENIC	homozygous	115344428
12	47583794	47583795	A	G	27	GENIC	homozygous	115344432
12	47584252	47584253	G	A	27	GENIC	homozygous	115444234
12	47584752	47584753	T	G	33	GENIC	homozygous	115344434
12	47584846	47584847	A	G	28	GENIC	homozygous	115344436
12	47584858	47584859	A	G	24	GENIC	homozygous	115344438
12	47584976	47584977	G	A	46	GENIC	homozygous	115344440
12	47587859	47587860	C	G	33	GENIC	homozygous	115344442
12	47580808	47580809	C	G	27	GENIC	homozygous	115516138