chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59156269	59156270	A	G	23	GENIC	homozygous	113820328
5	59157032	59157033	A	G	35	GENIC	homozygous	113820330
5	59157037	59157037		TCTCTG	34	GENIC	homozygous	128188344
5	59158651	59158652	C	A	16	GENIC	possibly homozygous	113820332
5	59163752	59163752		ATCT	7	GENIC	heterozygous	132075430
5	59164714	59164714		T	20	GENIC	homozygous	130551246
5	59164998	59164999	A	C	26	GENIC	homozygous	113820334
5	59157388	59157388		T	25	GENIC	possibly homozygous	130955116
5	59160741	59160741		A	20	GENIC	possibly homozygous	130955117
5	59157486	59157487	T	C	25	GENIC	homozygous	114118267
5	59162446	59162447	A	G	34	GENIC	homozygous	114118269