chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15984827	15984828	C	CTTTT	5	GENIC	heterozygous	52899652
9	15985272	15985273	C	T	22	GENIC	heterozygous	52338658
9	15988237	15988238	T	C	22	GENIC	homozygous	51770122
9	15987936	15987937	G	GT	18	GENIC	heterozygous	51770120
9	15989919	15989921	AA	--	18	GENIC	heterozygous	52338663
9	15989920	15989921	A	-	18	GENIC	possibly homozygous	51770124
9	15994911	15994912	T	C	21	GENIC	heterozygous	51770149
9	15995199	15995200	A	G	26	GENIC	homozygous	51770151
9	15997851	15997852	T	TC	29	GENIC	homozygous	51770166
9	15998357	15998358	T	TGGACGCG	32	GENIC	homozygous	51770168
9	15989583	15989584	C	T	22	GENIC	possibly homozygous	53647931
9	15994519	15994520	T	G	4	GENIC	homozygous	53647932
9	15992113	15992114	C	CTT	7	GENIC	heterozygous	53233917
9	16006748	16006749	A	G	21	GENIC	homozygous	51770188