chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	115863117	115863118	T	C	52	GENIC	homozygous	110967313
2	115866042	115866043	A	C	41	GENIC	homozygous	109988561
2	115866883	115866884	C	A	40	GENIC	possibly homozygous	110967315
2	115867897	115867898	C	T	32	GENIC	homozygous	109988568
2	115869131	115869132	G	T	32	GENIC	possibly homozygous	110967317
2	115869866	115869867	C	A	59	GENIC	homozygous	109988578
2	115872272	115872273	A	G	35	GENIC	homozygous	109988590
2	115875076	115875077	G	A	42	GENIC	homozygous	110967319
2	115876239	115876240	A	G	22	GENIC	homozygous	109988602
2	115877240	115877241	T	C	54	GENIC	possibly homozygous	110967321
2	115885838	115885839	C	G	42	GENIC	homozygous	109988622
2	115887019	115887020	A	C	51	GENIC	homozygous	109988626
2	115887991	115887992	A	C	28	GENIC	homozygous	109988627
2	115888567	115888568	C	T	32	GENIC	homozygous	110967323
2	115890950	115890951	C	T	29	GENIC	possibly homozygous	110967325
2	115891181	115891182	A	G	26	GENIC	homozygous	109988634