chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40256018	40256019	T	C	43	GENIC	homozygous	116568895
10	40258939	40258940	C	T	37	GENIC	homozygous	116568897
10	40259135	40259136	G	A	23	GENIC	homozygous	117057569
10	40263876	40263877	G	T	62	GENIC	homozygous	116568899
10	40264368	40264369	A	G	48	GENIC	homozygous	116568901
10	40264857	40264858	T	C	57	GENIC	homozygous	116568903
10	40265397	40265398	A	G	57	GENIC	homozygous	116568905
10	40266006	40266007	C	T	47	GENIC	homozygous	116568907
10	40267053	40267054	G	A	70	GENIC	possibly homozygous	116568909
10	40271009	40271010	G	C	64	GENIC	homozygous	116568911
10	40271211	40271212	G	A	65	GENIC	homozygous	116568913
10	40279159	40279160	G	A	53	GENIC	possibly homozygous	116568915
10	40279949	40279950	C	T	52	GENIC	homozygous	116568917
10	40280541	40280542	G	A	53	GENIC	homozygous	117990097
10	40280808	40280809	A	G	55	GENIC	homozygous	116568921
10	40281916	40281917	C	A	44	GENIC	homozygous	116568923
10	40281934	40281935	C	A	34	GENIC	homozygous	116568925
10	40284775	40284776	A	G	74	GENIC	homozygous	116568927
10	40291801	40291802	A	G	46	GENIC	heterozygous	117990098
10	40291891	40291892	G	T	66	GENIC	homozygous	116568929
10	40295869	40295870	T	A	78	GENIC	possibly homozygous	116568931
10	40296115	40296116	A	G	43	GENIC	homozygous	116568933
10	40296545	40296546	G	A	55	GENIC	possibly homozygous	116568935
10	40296928	40296929	A	G	49	GENIC	homozygous	116568943
10	40297031	40297032	T	G	50	GENIC	homozygous	116568945
10	40297833	40297834	T	C	47	GENIC	homozygous	116568947
10	40298427	40298428	G	A	57	GENIC	homozygous	116568949
10	40302058	40302059	C	T	41	GENIC	homozygous	116568951