chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40017956	40017957	A	G	12	GENIC	homozygous	52963642
8	40018311	40018312	T	A	15	GENIC	homozygous	52963643
8	40018610	40018611	A	T	12	GENIC	homozygous	52963644
8	40018640	40018641	T	TTGCCTCTATGGG	10	GENIC	homozygous	52592037
8	40019099	40019100	C	T	14	GENIC	homozygous	52963645
8	40019727	40019728	T	C	10	GENIC	homozygous	52963646
8	40020460	40020461	G	A	11	GENIC	homozygous	52963650
8	40020863	40020864	C	T	18	GENIC	homozygous	52963651
8	40020976	40020977	A	G	18	GENIC	homozygous	52963652
8	40021229	40021230	C	T	20	GENIC	homozygous	52963653
8	40022831	40022832	G	A	16	GENIC	homozygous	52963656
8	40023001	40023002	G	A	8	GENIC	homozygous	52592043
8	40023154	40023155	T	C	13	GENIC	homozygous	52963657
8	40023307	40023308	A	G	11	GENIC	homozygous	52592044
8	40023486	40023487	T	C	18	GENIC	homozygous	52963658
8	40023719	40023720	A	G	13	GENIC	homozygous	52592045