chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40186162	40186163	C	T	18	GENIC	homozygous	116568735
10	40186688	40186689	C	A	17	GENIC	homozygous	116568737
10	40187014	40187015	C	T	16	GENIC	homozygous	116568739
10	40187023	40187024	C	A	17	GENIC	homozygous	116568741
10	40187102	40187103	C	T	13	GENIC	homozygous	116763920
10	40188252	40188253	T	C	18	GENIC	homozygous	116763922
10	40189067	40189068	C	T	14	GENIC	homozygous	116763924
10	40192284	40192285	C	A	9	GENIC	heterozygous	116763928
10	40194533	40194534	T	C	11	GENIC	homozygous	116763930
10	40194580	40194581	A	G	21	GENIC	homozygous	116568745
10	40195183	40195184	G	A	13	GENIC	heterozygous	116763932
10	40195923	40195924	T	C	13	GENIC	homozygous	116763934
10	40196189	40196190	G	A	7	GENIC	homozygous	116763936
10	40197546	40197547	C	T	9	GENIC	homozygous	116763938
10	40192113	40192114	A	T	5	GENIC	homozygous	116870414