chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40262105	40262106	G	C	19	GENIC	homozygous	50422525
12	40262600	40262601	C	CTTTTTTT	4	GENIC	heterozygous	50543564
12	40262676	40262677	C	T	13	GENIC	homozygous	50422526
12	40262779	40262780	A	G	10	GENIC	homozygous	50543565
12	40263224	40263225	A	G	11	GENIC	homozygous	50422527
12	40263230	40263231	C	T	10	GENIC	homozygous	50422528
12	40263348	40263349	A	G	18	GENIC	homozygous	50202956
12	40263693	40263694	T	-	4	GENIC	heterozygous	50543566
12	40264362	40264363	T	A	11	GENIC	homozygous	50422530
12	40264442	40264443	G	A	18	GENIC	homozygous	50422531
12	40264808	40264809	T	C	6	GENIC	homozygous	50422532
12	40265417	40265418	T	C	29	GENIC	homozygous	50202959
12	40263692	40263694	TT	--	4	GENIC	heterozygous	50599305