chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40184260	40184261	G	T	51	GENIC	possibly homozygous	116568729
10	40184371	40184372	A	C	55	GENIC	homozygous	116568731
10	40185322	40185323	G	A	53	GENIC	homozygous	116568733
10	40186162	40186163	C	T	41	GENIC	homozygous	116568735
10	40186688	40186689	C	A	66	GENIC	homozygous	116568737
10	40187014	40187015	C	T	55	GENIC	homozygous	116568739
10	40187023	40187024	C	A	55	GENIC	homozygous	116568741
10	40187280	40187281	T	C	71	GENIC	possibly homozygous	116568743
10	40192113	40192114	A	T	28	GENIC	homozygous	116870414
10	40194580	40194581	A	G	41	GENIC	homozygous	116568745
10	40197548	40197549	C	T	59	GENIC	homozygous	117990087
10	40199426	40199427	A	G	57	GENIC	possibly homozygous	117990088
10	40200278	40200279	C	T	38	GENIC	possibly homozygous	116568747