chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40262105	40262106	G	C	28	GENIC	possibly homozygous	50422525
12	40262676	40262677	C	T	3	GENIC	homozygous	50422526
12	40263224	40263225	A	G	10	GENIC	homozygous	50422527
12	40263230	40263231	C	T	13	GENIC	homozygous	50422528
12	40263348	40263349	A	G	23	GENIC	possibly homozygous	50202956
12	40264362	40264363	T	A	29	GENIC	homozygous	50422530
12	40264442	40264443	G	A	28	GENIC	homozygous	50422531
12	40264808	40264809	T	C	16	GENIC	possibly homozygous	50422532
12	40265417	40265418	T	C	29	GENIC	homozygous	50202959