chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	171971646	171971647	C	T	45	GENIC	possibly homozygous	108379727
1	171971963	171971964	A	G	39	GENIC	homozygous	108379731
1	171972284	171972285	A	G	34	GENIC	homozygous	108379733
1	171972534	171972535	G	T	34	GENIC	homozygous	109347348
1	171972541	171972542	A	G	31	GENIC	homozygous	108379739
1	171973360	171973361	G	A	19	GENIC	homozygous	109347350
1	171974675	171974676	T	G	13	GENIC	homozygous	108379741
1	171975068	171975069	G	A	16	GENIC	homozygous	108959902
1	171975530	171975531	A	G	28	GENIC	homozygous	108379749
1	171977857	171977858	T	A	24	GENIC	homozygous	108959903
1	171979790	171979791	T	C	37	GENIC	homozygous	108379757
1	171980529	171980530	T	A	29	GENIC	homozygous	109347352
1	171980791	171980792	G	A	29	GENIC	homozygous	108379763
1	171980893	171980894	C	T	20	GENIC	homozygous	108379765