chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	48646936	48646936		AAAC	38	GENIC	homozygous	131501691
13	48647966	48647967	C		15	GENIC	homozygous	129051759
13	48647988	48647988		G	15	GENIC	homozygous	129051760
13	48648026	48648026		C	22	GENIC	homozygous	129051761
13	48648044	48648044		C	21	GENIC	homozygous	129051762
13	48648054	48648054		C	21	GENIC	homozygous	129051763
13	48648068	48648068		A	20	GENIC	homozygous	129051764
13	48648072	48648072		C	20	GENIC	homozygous	129051765
13	48648099	48648101	CG		13	GENIC	homozygous	131501692
13	48648104	48648119	TGTGATACGGAATCC		13	GENIC	homozygous	131501693
13	48648142	48648142		A	9	GENIC	homozygous	129051766
13	48648152	48648152		G	6	GENIC	homozygous	129051767
13	48648314	48648315	T		11	GENIC	homozygous	129051768
13	48648325	48648326	G		11	GENIC	homozygous	129051769
13	48649249	48649249		A	45	GENIC	homozygous	131501697
13	48650149	48650150	G	A	49	GENIC	homozygous	114549470
13	48648936	48648937	C	T	34	GENIC	homozygous	114549468
13	48649330	48649331	A	G	41	GENIC	homozygous	114549469