chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49441648	49441649	C	G	27	GENIC	homozygous	116488361
8	49441731	49441732	T	C	27	GENIC	homozygous	116488363
8	49443110	49443111	A	G	28	GENIC	homozygous	116488365
8	49443245	49443246	A	G	60	GENIC	homozygous	116488367
8	49443389	49443390	G	A	59	GENIC	homozygous	116488369
8	49444743	49444744	A	T	33	GENIC	homozygous	116488371
8	49446786	49446787	T	C	33	GENIC	homozygous	116488373
8	49446788	49446789	A	G	34	GENIC	homozygous	116488375
8	49446795	49446796	T	C	32	GENIC	homozygous	116488377
8	49447317	49447318	A	G	53	GENIC	homozygous	116488379
8	49448903	49448904	A	G	37	GENIC	homozygous	116488381
8	49450238	49450239	A	G	11	GENIC	homozygous	117142034
8	49450671	49450672	G	A	37	GENIC	homozygous	116488383
8	49450672	49450673	T	C	38	GENIC	homozygous	116488385
8	49450743	49450744	A	C	32	GENIC	homozygous	116488387