chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	15445334	15445335	G	A	19	GENIC	homozygous	111454719
3	15446007	15446008	T	C	30	GENIC	homozygous	111454720
3	15448974	15448975	A	G	27	GENIC	homozygous	111454721
3	15449038	15449039	T	C	25	GENIC	homozygous	111454722
3	15449070	15449071	G	A	19	GENIC	homozygous	111454723
3	15449388	15449389	A	G	28	GENIC	homozygous	111454724
3	15450061	15450062	G	A	25	GENIC	homozygous	111454725
3	15450426	15450427	C	T	21	GENIC	homozygous	111454726
3	15450537	15450538	C	T	32	GENIC	homozygous	111454727
3	15450681	15450682	C	T	37	GENIC	homozygous	111454728
3	15451493	15451494	G	A	47	GENIC	homozygous	111454729
3	15451524	15451525	T	C	47	GENIC	homozygous	111454730
3	15452835	15452836	C	A	38	GENIC	homozygous	111454731
3	15453498	15453499	A	T	40	GENIC	homozygous	111454732
3	15453967	15453968	G	A	25	GENIC	homozygous	111454733
3	15455805	15455806	T	C	31	GENIC	homozygous	112223611
3	15456426	15456427	G	A	31	GENIC	homozygous	111454734
3	15456877	15456878	C	T	41	GENIC	homozygous	111454735
3	15457571	15457572	A	T	29	GENIC	homozygous	111454736
3	15458903	15458904	C	T	29	GENIC	homozygous	111454737
3	15460900	15460901	A	C	27	GENIC	homozygous	111454738
3	15461788	15461789	A	T	18	GENIC	homozygous	111454739
3	15462174	15462175	C	G	24	GENIC	homozygous	111454740
3	15462997	15462998	C	G	32	GENIC	homozygous	111454741
3	15462998	15462999	C	G	32	GENIC	homozygous	111454742