chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123731705	123731706	T	G	43	GENIC	homozygous	111692722
3	123733602	123733603	G	A	50	GENIC	homozygous	111692724
3	123734009	123734010	A	G	59	GENIC	homozygous	111692725
3	123734953	123734954	T	C	44	GENIC	homozygous	111692726
3	123735516	123735517	A	G	54	GENIC	homozygous	111692728
3	123735673	123735674	G	A	35	GENIC	homozygous	111692729
3	123736910	123736911	A	G	57	GENIC	homozygous	111692730
3	123738288	123738289	C	G	58	GENIC	homozygous	111692731
3	123738615	123738616	T	C	56	GENIC	homozygous	111692732
3	123739036	123739037	A	T	59	GENIC	homozygous	111692733
3	123739039	123739040	T	A	60	GENIC	homozygous	111692734
3	123739354	123739355	A	G	49	GENIC	homozygous	111692735
3	123739499	123739500	G	T	42	GENIC	homozygous	111692736
3	123739668	123739669	T	C	47	GENIC	homozygous	111692737
3	123740036	123740037	C	T	55	GENIC	homozygous	111692738
3	123740230	123740231	A	G	48	GENIC	homozygous	111692739
3	123740592	123740593	G	A	55	GENIC	homozygous	111692740
3	123740766	123740767	T	C	50	GENIC	homozygous	111692741
3	123736914	123736914		A	58	GENIC	homozygous	127925835
3	123733279	123733280	T		34	GENIC	heterozygous	131627783
3	123733271	123733272	T		34	GENIC	possibly homozygous	127925833
3	123734190	123734191	A		41	GENIC	heterozygous	127925834
3	123737968	123737968		G	49	GENIC	homozygous	127925836
3	123733275	123733276	T		34	GENIC	possibly homozygous	131627782