chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123731705	123731706	T	G	13	GENIC	homozygous	111692722
3	123733265	123733265		A	12	GENIC	homozygous	134525893
3	123733602	123733603	G	A	27	GENIC	homozygous	111692724
3	123734953	123734954	T	C	20	GENIC	homozygous	111692726
3	123735031	123735031		GGTT	24	GENIC	homozygous	134525894
3	123735516	123735517	A	G	23	GENIC	homozygous	111692728
3	123736242	123736243	C	T	17	GENIC	homozygous	112447465
3	123736310	123736311	C	T	15	GENIC	homozygous	120084349
3	123736910	123736911	A	G	19	GENIC	homozygous	111692730
3	123736914	123736914		A	20	GENIC	homozygous	127925835
3	123737968	123737968		G	29	GENIC	homozygous	127925836
3	123738288	123738289	C	G	29	GENIC	homozygous	111692731
3	123738615	123738616	T	C	22	GENIC	homozygous	111692732
3	123739036	123739037	A	T	24	GENIC	homozygous	111692733
3	123739039	123739040	T	A	24	GENIC	homozygous	111692734
3	123739354	123739355	A	G	23	GENIC	homozygous	111692735
3	123739499	123739500	G	T	28	GENIC	homozygous	111692736
3	123739668	123739669	T	C	19	GENIC	homozygous	111692737
3	123740036	123740037	C	T	21	GENIC	homozygous	111692738
3	123740230	123740231	A	G	19	GENIC	homozygous	111692739
3	123740592	123740593	G	A	30	GENIC	homozygous	111692740
3	123740766	123740767	T	C	18	GENIC	homozygous	111692741