chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	160800069	160800070	G	T	11	GENIC	homozygous	111794669
3	160800318	160800319	C	A	9	GENIC	homozygous	111794671
3	160800333	160800334	C	T	6	GENIC	homozygous	111794673
3	160800377	160800378	C	G	12	GENIC	homozygous	111794675
3	160800432	160800433	T	A	4	GENIC	homozygous	111794679
3	160800541	160800542	G	T	7	GENIC	homozygous	111794683
3	160800690	160800691	A	G	5	GENIC	homozygous	111794685
3	160800732	160800733	G	T	6	GENIC	homozygous	121903523
3	160800762	160800763	G	C	7	GENIC	homozygous	111794687
3	160801080	160801081	A	T	7	GENIC	homozygous	111794697
3	160801117	160801118	G	A	4	GENIC	homozygous	111794699
3	160801385	160801386	T	C	12	GENIC	homozygous	111794725
3	160801427	160801428	C	T	12	GENIC	homozygous	111794727
3	160801544	160801545	A	G	10	GENIC	homozygous	111794733
3	160801584	160801585	A	G	6	GENIC	homozygous	111794735
3	160801635	160801636	A	G	11	GENIC	homozygous	111794737
3	160801669	160801670	G	A	13	GENIC	homozygous	111794739
3	160801689	160801690	A	G	10	GENIC	homozygous	111794741
3	160801753	160801754	G	C	13	GENIC	homozygous	111794743
3	160801759	160801760	G	A	13	GENIC	homozygous	111794745
3	160801808	160801809	G	C	14	GENIC	homozygous	111794747
3	160801862	160801863	A	G	9	GENIC	homozygous	111794749
3	160802121	160802122	C	T	18	GENIC	homozygous	111794753