chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40262105	40262106	G	C	25	GENIC	homozygous	50422525
12	40262600	40262601	C	CT	6	GENIC	homozygous	50202955
12	40262619	40262620	C	T	8	GENIC	heterozygous	50381633
12	40262676	40262677	C	T	14	GENIC	homozygous	50422526
12	40263224	40263225	A	G	37	GENIC	homozygous	50422527
12	40263230	40263231	C	T	37	GENIC	homozygous	50422528
12	40263348	40263349	A	G	27	GENIC	homozygous	50202956
12	40263692	40263693	T	-	1	GENIC	homozygous	50422529
12	40264362	40264363	T	A	40	GENIC	homozygous	50422530
12	40264442	40264443	G	A	37	GENIC	homozygous	50422531
12	40264808	40264809	T	C	42	GENIC	homozygous	50422532
12	40265417	40265418	T	C	15	GENIC	homozygous	50202959