chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	105097046	105097047	C	T	13	GENIC	homozygous	108905899
1	105097056	105097057	A	G	12	GENIC	homozygous	108905900
1	105097862	105097863	C	G	65	GENIC	homozygous	108905901
1	105098036	105098037	C	T	49	GENIC	homozygous	108905902
1	105098212	105098213	C	T	56	GENIC	homozygous	108905903
1	105098340	105098341	G	A	42	GENIC	homozygous	108905904
1	105099089	105099091	GT		40	GENIC	heterozygous	130211066
1	105099604	105099605	C	T	56	GENIC	homozygous	108905905
1	105099710	105099711	A	G	64	GENIC	homozygous	108905906
1	105100184	105100185	C	T	45	GENIC	homozygous	108905907
1	105103652	105103653	T	C	42	GENIC	homozygous	108905911
1	105100832	105100833	A	G	50	GENIC	homozygous	108905908
1	105101832	105101833	T	C	60	GENIC	homozygous	108905909
1	105103632	105103633	T	C	44	GENIC	homozygous	108905910
1	105103919	105103920	G	A	42	GENIC	homozygous	108905912
1	105107551	105107552	A	G	58	GENIC	homozygous	108905915
1	105107638	105107639	A	G	64	GENIC	homozygous	108905916
1	105107943	105107944	T	C	52	GENIC	homozygous	108905917
1	105108957	105108958	T	C	72	GENIC	homozygous	108905918
1	105108293	105108293		T	29	GENIC	homozygous	130819268
1	105105543	105105543		C	50	GENIC	homozygous	130819266
1	105105929	105105943	GTGTGGTGTCACTT		48	GENIC	homozygous	130819267