chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49441648	49441649	C	G	58	GENIC	possibly homozygous	116488361
8	49441731	49441732	T	C	51	GENIC	possibly homozygous	116488363
8	49441759	49441762	AGA		53	GENIC	possibly homozygous	128588843
8	49443110	49443111	A	G	52	GENIC	homozygous	116488365
8	49443245	49443246	A	G	61	GENIC	homozygous	116488367
8	49443389	49443390	G	A	52	GENIC	homozygous	116488369
8	49444743	49444744	A	T	66	GENIC	homozygous	116488371
8	49446786	49446787	T	C	53	GENIC	homozygous	116488373
8	49446788	49446789	A	G	53	GENIC	homozygous	116488375
8	49446795	49446796	T	C	50	GENIC	homozygous	116488377
8	49447317	49447318	A	G	62	GENIC	homozygous	116488379
8	49448735	49448740	AAAAC		27	GENIC	homozygous	128588844
8	49448903	49448904	A	G	49	GENIC	homozygous	116488381
8	49450671	49450672	G	A	51	GENIC	homozygous	116488383
8	49450672	49450673	T	C	52	GENIC	homozygous	116488385
8	49450743	49450744	A	C	45	GENIC	homozygous	116488387
8	49450750	49450758	CATTGTTT		45	GENIC	homozygous	128588846
8	49453733	49453733		T	44	GENIC	possibly homozygous	128588847