chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	168442553	168442554	G	A	64	GENIC	possibly homozygous	143795499
1	168442603	168442604	A	G	61	GENIC	homozygous	135740836
1	168443546	168443547	T	C	51	GENIC	homozygous	135740838
1	168443593	168443594	T	C	50	GENIC	homozygous	135740839
1	168444558	168444559	G	A	37	GENIC	homozygous	135740840
1	168445235	168445236	T	C	47	GENIC	homozygous	143795500
1	168445705	168445706	T	C	56	GENIC	homozygous	135740841
1	168445823	168445824	A	G	42	GENIC	homozygous	135740842
1	168446243	168446244	A	G	47	GENIC	homozygous	135740843
1	168446962	168446963	G	A	52	GENIC	homozygous	143795501
1	168447525	168447526	T	C	39	GENIC	homozygous	135740844
1	168448183	168448184	C	T	40	GENIC	homozygous	143795502
1	168448630	168448631	A	G	52	GENIC	homozygous	135740846
1	168450105	168450106	T	C	45	GENIC	homozygous	143795503
1	168450849	168450850	T	C	24	GENIC	homozygous	135740848
1	168451059	168451060	G	A	52	GENIC	homozygous	143795504
1	168451073	168451074	G	A	56	GENIC	homozygous	143795505
1	168451087	168451088	A	C	58	GENIC	homozygous	135740849
1	168451473	168451474	G	A	51	GENIC	homozygous	143795506
1	168452017	168452018	T	C	52	GENIC	homozygous	135740850
1	168452417	168452418	T	C	38	GENIC	homozygous	143795507
1	168452606	168452607	T	C	52	GENIC	homozygous	135740851
1	168452783	168452784	C	G	56	GENIC	homozygous	135740852
1	168453160	168453161	C	A	72	GENIC	homozygous	135740853
1	168451036	168451038	TC		46	GENIC	homozygous	143742467
1	168445691	168445692	C		59	GENIC	homozygous	143742465
1	168447941	168447942	T		32	GENIC	possibly homozygous	143742466