chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59981745	59981746	T	G	30	GENIC	homozygous	52665814
8	59981829	59981830	A	G	37	GENIC	homozygous	52665816
8	59984237	59984238	T	G	25	GENIC	homozygous	52665818
8	59984427	59984428	T	TACAC	8	GENIC	homozygous	52665822
8	59984958	59984959	A	G	26	GENIC	homozygous	52665826
8	59985039	59985040	T	C	25	GENIC	homozygous	52665832
8	59985452	59985453	C	T	27	GENIC	homozygous	53300237
8	59985738	59985739	A	G	17	GENIC	homozygous	52665836
8	59985956	59985957	C	T	21	GENIC	possibly homozygous	53300238
8	59986096	59986097	T	C	24	GENIC	homozygous	52665842
8	59987014	59987015	T	C	33	GENIC	homozygous	52665844
8	59987061	59987062	C	G	38	GENIC	homozygous	52665846
8	59987111	59987112	G	-	34	GENIC	homozygous	53300239
8	59987242	59987243	T	C	30	GENIC	homozygous	52665848
8	59987772	59987773	T	-	31	GENIC	homozygous	53300240
8	59989874	59989875	A	C	11	GENIC	homozygous	52665850
8	59990401	59990402	G	A	28	GENIC	homozygous	53300241
8	59990601	59990602	C	CG	22	GENIC	homozygous	53300243
8	59991769	59991770	T	C	17	GENIC	homozygous	52665858