chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123731705	123731706	T	G	31	GENIC	homozygous	111692722
3	123733271	123733272	T	A	4	GENIC	homozygous	112447462
3	123733275	123733276	T	A	4	GENIC	homozygous	112147617
3	123733279	123733280	T	A	4	GENIC	homozygous	111692723
3	123733602	123733603	G	A	21	GENIC	homozygous	111692724
3	123734009	123734010	A	G	19	GENIC	homozygous	111692725
3	123734953	123734954	T	C	29	GENIC	homozygous	111692726
3	123734984	123734985	C	T	25	GENIC	homozygous	111692727
3	123735516	123735517	A	G	23	GENIC	homozygous	111692728
3	123735673	123735674	G	A	28	GENIC	homozygous	111692729
3	123738288	123738289	C	G	27	GENIC	homozygous	111692731
3	123738615	123738616	T	C	35	GENIC	homozygous	111692732
3	123739036	123739037	A	T	37	GENIC	homozygous	111692733
3	123739039	123739040	T	A	35	GENIC	homozygous	111692734
3	123739354	123739355	A	G	29	GENIC	homozygous	111692735
3	123739499	123739500	G	T	25	GENIC	homozygous	111692736
3	123739668	123739669	T	C	34	GENIC	homozygous	111692737
3	123740036	123740037	C	T	43	GENIC	homozygous	111692738
3	123740230	123740231	A	G	35	GENIC	homozygous	111692739
3	123740592	123740593	G	A	38	GENIC	homozygous	111692740
3	123740766	123740767	T	C	23	GENIC	homozygous	111692741
3	123741334	123741335	T	A	38	GENIC	homozygous	111692742