chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40262600	40262601	C	CT	19	GENIC	heterozygous	50202955
12	40262619	40262620	C	T	29	GENIC	heterozygous	50381633
12	40263348	40263349	A	G	29	GENIC	homozygous	50202956
12	40265417	40265418	T	C	22	GENIC	homozygous	50202959
12	40264314	40264315	G	A	27	GENIC	homozygous	50452186