chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	63221395	63221396	T	C	15	GENIC	homozygous	111911532
3	63221476	63221477	A	G	27	GENIC	homozygous	111911533
3	63221798	63221799	A	G	18	GENIC	homozygous	111911534
3	63222043	63222044	C	T	24	GENIC	possibly homozygous	111911535
3	63222249	63222250	T	C	21	GENIC	homozygous	111911537
3	63224590	63224591	G	A	24	GENIC	homozygous	111911538
3	63224771	63224772	A	G	24	GENIC	homozygous	111911539
3	63225285	63225286	T	C	12	GENIC	homozygous	111911540
3	63225634	63225635	A	G	22	GENIC	homozygous	111911541
3	63226461	63226462	A	G	23	GENIC	homozygous	111911542
3	63227218	63227219	G	T	14	GENIC	homozygous	111911543
3	63228337	63228338	A	G	15	GENIC	homozygous	111911544
3	63228621	63228622	T	C	19	GENIC	homozygous	111911545
3	63228712	63228713	C	T	16	GENIC	homozygous	111911546
3	63229060	63229061	C	T	13	GENIC	homozygous	111911547
3	63230423	63230424	C	T	15	GENIC	homozygous	111911550
3	63231952	63231953	A	G	18	GENIC	homozygous	111911552
3	63232277	63232278	T	G	26	GENIC	homozygous	111911553
3	63232440	63232441	C	A	28	GENIC	homozygous	111911554
3	63232681	63232682	T	C	15	GENIC	homozygous	111911555
3	63232685	63232686	T	C	12	GENIC	homozygous	111911556
3	63232852	63232853	A	G	13	GENIC	heterozygous	111911557
3	63232957	63232958	C	T	13	GENIC	homozygous	111911558
3	63233046	63233047	C	T	13	GENIC	homozygous	111911559
3	63233175	63233176	C	T	18	GENIC	homozygous	111911560
3	63233382	63233383	A	G	19	GENIC	homozygous	111911561
3	63233760	63233761	C	T	12	GENIC	homozygous	111911562
3	63234043	63234044	G	A	29	GENIC	homozygous	111911563
3	63234795	63234796	T	C	27	GENIC	homozygous	111911564
3	63235190	63235191	G	A	14	GENIC	homozygous	111911565