chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40262600	40262601	C	CT	8	GENIC	heterozygous	50202955
12	40263348	40263349	A	G	30	GENIC	homozygous	50202956
12	40263498	40263499	A	AT	25	GENIC	homozygous	50202957
12	40263691	40263692	G	GT	8	GENIC	possibly homozygous	50611755
12	40263691	40263692	G	GTT	8	GENIC	heterozygous	50571675
12	40264987	40264988	T	C	24	GENIC	homozygous	50202958
12	40265417	40265418	T	C	49	GENIC	homozygous	50202959