chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40016315	40016316	C	CTT	2	GENIC	homozygous	52963640
8	40017956	40017957	A	G	24	GENIC	homozygous	52963642
8	40018311	40018312	T	A	16	GENIC	homozygous	52963643
8	40018408	40018411	AAA	---	4	GENIC	homozygous	52592036
8	40018610	40018611	A	T	16	GENIC	homozygous	52963644
8	40018640	40018641	T	TTGCCTCTATGGG	18	GENIC	homozygous	52592037
8	40019099	40019100	C	T	30	GENIC	homozygous	52963645
8	40019727	40019728	T	C	28	GENIC	homozygous	52963646
8	40019826	40019827	G	GT	14	GENIC	heterozygous	52592039
8	40019826	40019827	G	GTT	14	GENIC	possibly homozygous	52963647
8	40020054	40020055	G	GT	12	GENIC	homozygous	52963648
8	40020069	40020070	C	CTT	2	GENIC	heterozygous	52963649
8	40020069	40020070	C	CT	2	GENIC	heterozygous	53550279
8	40020460	40020461	G	A	31	GENIC	homozygous	52963650
8	40020863	40020864	C	T	38	GENIC	homozygous	52963651
8	40020976	40020977	A	G	32	GENIC	homozygous	52963652
8	40021229	40021230	C	T	17	GENIC	homozygous	52963653
8	40022648	40022649	T	TG	9	GENIC	heterozygous	52592042
8	40022648	40022649	T	TGG	9	GENIC	possibly homozygous	52963654
8	40022676	40022677	A	G	25	GENIC	homozygous	52963655
8	40022831	40022832	G	A	25	GENIC	homozygous	52963656
8	40023001	40023002	G	A	19	GENIC	homozygous	52592043
8	40023154	40023155	T	C	54	GENIC	homozygous	52963657
8	40023307	40023308	A	G	52	GENIC	homozygous	52592044
8	40023486	40023487	T	C	51	GENIC	homozygous	52963658
8	40023719	40023720	A	G	57	GENIC	homozygous	52592045