chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	105097046	105097047	C	T	18	GENIC	heterozygous	108905899
1	105097056	105097057	A	G	14	GENIC	heterozygous	108905900
1	105097862	105097863	C	G	33	GENIC	homozygous	108905901
1	105098036	105098037	C	T	28	GENIC	homozygous	108905902
1	105098212	105098213	C	T	18	GENIC	homozygous	108905903
1	105098340	105098341	G	A	20	GENIC	homozygous	108905904
1	105099604	105099605	C	T	29	GENIC	homozygous	108905905
1	105099710	105099711	A	G	25	GENIC	homozygous	108905906
1	105100184	105100185	C	T	30	GENIC	homozygous	108905907
1	105100832	105100833	A	G	27	GENIC	homozygous	108905908
1	105101832	105101833	T	C	23	GENIC	homozygous	108905909
1	105103632	105103633	T	C	11	GENIC	homozygous	108905910
1	105103652	105103653	T	C	15	GENIC	homozygous	108905911
1	105103919	105103920	G	A	21	GENIC	homozygous	108905912
1	105105415	105105416	G	T	15	GENIC	homozygous	109046775
1	105105942	105105943	T	C	45	GENIC	homozygous	108905913
1	105106727	105106728	C	T	20	GENIC	homozygous	108905914
1	105107551	105107552	A	G	32	GENIC	homozygous	108905915
1	105107638	105107639	A	G	30	GENIC	homozygous	108905916
1	105107943	105107944	T	C	16	GENIC	homozygous	108905917
1	105108957	105108958	T	C	28	GENIC	homozygous	108905918