chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	190556105	190556106	G	T	22	GENIC	homozygous	108465670
1	190556305	190556306	C	A	13	GENIC	homozygous	108465671
1	190558447	190558448	G	A	20	GENIC	homozygous	109178260
1	190558475	190558476	G	A	23	GENIC	homozygous	108465674
1	190559222	190559223	T	C	27	GENIC	homozygous	108465675
1	190565578	190565579	T	A	14	GENIC	homozygous	108465678
1	190567366	190567367	G	C	17	GENIC	homozygous	108465679
1	190567371	190567372	C	G	17	GENIC	homozygous	108465680
1	190567387	190567388	T	A	20	GENIC	homozygous	108465681
1	190567437	190567438	A	G	26	GENIC	homozygous	108465682
1	190568784	190568785	A	G	23	GENIC	homozygous	108465683
1	190571401	190571402	C	T	13	GENIC	homozygous	108465684
1	190572977	190572978	C	T	17	GENIC	homozygous	108465685
1	190573826	190573827	C	T	22	GENIC	homozygous	108465686
1	190574019	190574020	A	G	21	GENIC	homozygous	108465687
1	190574020	190574021	A	G	21	GENIC	homozygous	108465688
1	190575402	190575403	G	A	4	GENIC	homozygous	108763723
1	190575439	190575440	G	T	2	GENIC	homozygous	108763724
1	190576988	190576989	C	G	12	GENIC	homozygous	108465690
1	190577116	190577117	T	C	7	GENIC	homozygous	108465691
1	190579958	190579959	G	A	18	GENIC	homozygous	109178265
1	190580576	190580577	G	T	24	GENIC	homozygous	108465701
1	190580762	190580763	A	G	21	GENIC	homozygous	108465702
1	190582759	190582760	T	A	23	GENIC	homozygous	108465703
1	190582867	190582868	G	A	17	GENIC	homozygous	108465704
1	190584625	190584626	C	T	20	GENIC	homozygous	108465705