chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	2665591	2665591		A	39	GENIC	homozygous	138232698
8	2666797	2666797		C	43	GENIC	possibly homozygous	138232699
8	2666847	2666848	A		40	GENIC	homozygous	138232700
8	2666876	2666876		T	34	GENIC	homozygous	138232701
8	2667033	2667033		T	33	GENIC	homozygous	138232702
8	2667069	2667069		T	27	GENIC	homozygous	138232703
8	2667218	2667219	C		40	GENIC	homozygous	138232704
8	2667236	2667237	A		42	GENIC	homozygous	138232705
8	2667325	2667326	A		38	GENIC	homozygous	138232706
8	2667454	2667454		T	51	GENIC	homozygous	138232707
8	2667539	2667539		A	44	GENIC	homozygous	138232708
8	2668115	2668115		G	41	GENIC	homozygous	138232709
8	2668135	2668136	C		45	GENIC	homozygous	138232710
8	2668200	2668201	A		37	GENIC	homozygous	138232711
8	2668446	2668446		A	47	GENIC	homozygous	138232712
8	2668488	2668489	A		47	GENIC	homozygous	138232713
8	2668512	2668512		G	49	GENIC	homozygous	138232714
8	2668980	2668981	T		51	GENIC	homozygous	138232715