chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	171971646	171971647	C	T	55	GENIC	homozygous	108379727
1	171971771	171971772	A	G	38	GENIC	homozygous	108379729
1	171971963	171971964	A	G	58	GENIC	homozygous	108379731
1	171972284	171972285	A	G	49	GENIC	homozygous	108379733
1	171972451	171972452	A	C	61	GENIC	homozygous	108379735
1	171972458	171972459	A	C	64	GENIC	homozygous	108379737
1	171972541	171972542	A	G	52	GENIC	homozygous	108379739
1	171974675	171974676	T	G	31	GENIC	heterozygous	108379741
1	171974691	171974692	G	T	33	GENIC	heterozygous	108379743
1	171974722	171974723	T	C	43	GENIC	homozygous	108379745
1	171974752	171974753	A	G	34	GENIC	homozygous	108379747
1	171975530	171975531	A	G	59	GENIC	possibly homozygous	108379749
1	171975637	171975638	A	G	52	GENIC	homozygous	108379751
1	171976667	171976668	T	C	37	GENIC	homozygous	108379753
1	171977687	171977688	C	T	54	GENIC	homozygous	108379755
1	171979790	171979791	T	C	39	GENIC	homozygous	108379757
1	171980438	171980439	G	T	57	GENIC	homozygous	108379759
1	171980741	171980742	T	A	53	GENIC	homozygous	108379761
1	171980791	171980792	G	A	53	GENIC	homozygous	108379763
1	171980893	171980894	C	T	44	GENIC	homozygous	108379765
1	171981306	171981307	T	G	43	GENIC	homozygous	108379767