chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	112340342	112340342		G	13	GENIC	homozygous	127919117
3	112341054	112341055	G	A	7	GENIC	homozygous	111675575
3	112341687	112341688	C	T	11	GENIC	homozygous	111675576
3	112342273	112342273		G	15	GENIC	homozygous	127919118
3	112342283	112342283		T	14	GENIC	homozygous	127919119
3	112344444	112344444		T	11	GENIC	homozygous	130908198
3	112346136	112346137	A	G	20	GENIC	homozygous	111675579
3	112350764	112350768	TTTG		20	GENIC	homozygous	130908199
3	112350880	112350881	A	G	16	GENIC	homozygous	111675581
3	112346515	112346516	C	T	16	GENIC	homozygous	112006828
3	112346620	112346621	A	G	10	GENIC	homozygous	112006830
3	112351714	112351715	C	T	9	GENIC	homozygous	112006832
3	112352937	112352938	G	A	19	GENIC	homozygous	112006834
3	112353395	112353396	A	C	12	GENIC	homozygous	111675584
3	112353564	112353565	C	T	11	GENIC	homozygous	112006838
3	112353796	112353797	A	G	14	GENIC	homozygous	112006841
3	112354162	112354162		C	15	GENIC	homozygous	127919120
3	112355711	112355711		T	16	GENIC	homozygous	127919121
3	112355718	112355718		T	16	GENIC	homozygous	127919122
3	112355767	112355768	A		15	GENIC	homozygous	127919123
3	112355772	112355772		G	16	GENIC	homozygous	127919124
3	112359487	112359488	G	A	13	GENIC	homozygous	112006845
3	112362878	112362879	G	A	22	GENIC	homozygous	112006847