chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49441648	49441649	C	G	13	GENIC	homozygous	116488361
8	49441731	49441732	T	C	15	GENIC	homozygous	116488363
8	49441759	49441762	AGA		18	GENIC	homozygous	128588843
8	49443110	49443111	A	G	16	GENIC	homozygous	116488365
8	49443245	49443246	A	G	15	GENIC	homozygous	116488367
8	49443389	49443390	G	A	19	GENIC	homozygous	116488369
8	49444743	49444744	A	T	21	GENIC	homozygous	116488371
8	49446786	49446787	T	C	18	GENIC	homozygous	116488373
8	49446788	49446789	A	G	18	GENIC	homozygous	116488375
8	49446795	49446796	T	C	18	GENIC	homozygous	116488377
8	49447076	49447077	G	A	15	GENIC	heterozygous	131059575
8	49447317	49447318	A	G	18	GENIC	homozygous	116488379
8	49448735	49448740	AAAAC		7	GENIC	homozygous	128588844
8	49448903	49448904	A	G	15	GENIC	homozygous	116488381
8	49450671	49450672	G	A	6	GENIC	homozygous	116488383
8	49450672	49450673	T	C	6	GENIC	homozygous	116488385
8	49450743	49450744	A	C	9	GENIC	homozygous	116488387
8	49450750	49450758	CATTGTTT		9	GENIC	homozygous	128588846
8	49453733	49453733		T	24	GENIC	homozygous	128588847