chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	190555194	190555195	A	G	15	GENIC	homozygous	108465669
1	190556105	190556106	G	T	16	GENIC	homozygous	108465670
1	190556305	190556306	C	A	17	GENIC	homozygous	108465671
1	190557618	190557619	T	G	14	GENIC	homozygous	108465673
1	190558475	190558476	G	A	15	GENIC	homozygous	108465674
1	190561494	190561495	A	T	5	GENIC	homozygous	108465676
1	190564421	190564422	C	T	5	GENIC	heterozygous	125374516
1	190565578	190565579	T	A	9	GENIC	heterozygous	108465678
1	190567366	190567367	G	C	7	GENIC	homozygous	108465679
1	190567387	190567388	T	A	4	GENIC	homozygous	108465681
1	190567437	190567438	A	G	14	GENIC	homozygous	108465682
1	190568784	190568785	A	G	18	GENIC	homozygous	108465683
1	190571401	190571402	C	T	16	GENIC	homozygous	108465684
1	190572977	190572978	C	T	11	GENIC	homozygous	108465685
1	190573826	190573827	C	T	14	GENIC	homozygous	108465686
1	190574019	190574020	A	G	20	GENIC	homozygous	108465687
1	190574020	190574021	A	G	20	GENIC	homozygous	108465688
1	190576922	190576923	A	G	10	GENIC	homozygous	108465689
1	190576988	190576989	C	G	9	GENIC	homozygous	108465690
1	190579088	190579089	G	A	15	GENIC	homozygous	108465696
1	190579108	190579109	A	C	9	GENIC	homozygous	108465697
1	190579147	190579148	C	G	15	GENIC	homozygous	108465698
1	190580576	190580577	G	T	17	GENIC	homozygous	108465701
1	190580762	190580763	A	G	27	GENIC	homozygous	108465702
1	190582867	190582868	G	A	16	GENIC	homozygous	108465704
1	190584625	190584626	C	T	20	GENIC	homozygous	108465705