chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20846239	20846240	C	T	42	GENIC	homozygous	112228731
16	20849624	20849625	T	C	29	GENIC	possibly homozygous	111753662
16	20849983	20849984	G	A	15	GENIC	homozygous	111753664
16	20850135	20850136	G	A	33	GENIC	homozygous	111753666
16	20851244	20851245	G	A	5	GENIC	heterozygous	112292618
16	20851968	20851969	C	T	48	GENIC	homozygous	111753668
16	20852104	20852105	C	G	48	GENIC	homozygous	111753670
16	20852262	20852263	T	C	36	GENIC	homozygous	111753672
16	20852490	20852491	A	T	13	GENIC	homozygous	111753674
16	20852593	20852594	G	A	25	GENIC	homozygous	111753676
16	20853015	20853016	C	T	29	GENIC	homozygous	111753678
16	20853618	20853619	G	A	39	GENIC	homozygous	111753680
16	20854198	20854199	A	G	36	GENIC	homozygous	111753682
16	20854272	20854273	C	T	30	GENIC	homozygous	111753684
16	20854666	20854667	C	A	39	GENIC	homozygous	111753686
16	20855272	20855273	C	T	46	GENIC	homozygous	111753690
16	20855557	20855558	G	A	46	GENIC	homozygous	111753692
16	20855628	20855629	C	T	39	GENIC	homozygous	111753694
16	20858701	20858702	G	A	34	GENIC	homozygous	111948950
16	20850464	20850465	C	T	7	GENIC	homozygous	119192803
16	20855447	20855448	G	A	37	GENIC	homozygous	111948948