chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40262105	40262106	G	C	43	GENIC	homozygous	50422525
12	40262600	40262601	C	CT	24	GENIC	homozygous	50202955
12	40262619	40262620	C	T	37	GENIC	heterozygous	50381633
12	40262676	40262677	C	T	23	GENIC	possibly homozygous	50422526
12	40263224	40263225	A	G	34	GENIC	homozygous	50422527
12	40263230	40263231	C	T	35	GENIC	homozygous	50422528
12	40263348	40263349	A	G	46	GENIC	homozygous	50202956
12	40263692	40263693	T	-	5	GENIC	homozygous	50422529
12	40264362	40264363	T	A	28	GENIC	homozygous	50422530
12	40264442	40264443	G	A	26	GENIC	homozygous	50422531
12	40264808	40264809	T	C	24	GENIC	homozygous	50422532
12	40265417	40265418	T	C	43	GENIC	homozygous	50202959