chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	49921011	49921012	C		28	GENIC	homozygous	128710025
9	49967015	49967016	C	A	15	GENIC	homozygous	117539714
9	49967016	49967017	G	A	15	GENIC	homozygous	117539716
9	49967017	49967018	C	G	14	GENIC	homozygous	117539718
9	49967021	49967022	C		15	GENIC	homozygous	128710026
9	49967023	49967024	C		14	GENIC	homozygous	128710027
9	49986310	49986311	A		14	GENIC	homozygous	128710028
9	49986312	49986313	A		14	GENIC	homozygous	128710029
9	49986319	49986319		TTT	12	GENIC	homozygous	128710030
9	49986320	49986320		TG	11	GENIC	homozygous	128710031
9	49986322	49986322		GAT	11	GENIC	homozygous	128710032
9	49986323	49986325	GC		12	GENIC	homozygous	128710033
9	49986328	49986329	T		13	GENIC	homozygous	128710034
9	49986332	49986332		T	12	GENIC	homozygous	128710035
9	49986336	49986337	C		12	GENIC	homozygous	128710036
9	49986339	49986339		T	12	GENIC	homozygous	128710037
9	49986342	49986343	T	G	11	GENIC	homozygous	117539720
9	49986343	49986344	G	T	11	GENIC	homozygous	117539722
9	49986901	49986902	G	C	7	GENIC	homozygous	117539724
9	49986903	49986904	G	C	7	GENIC	homozygous	117539726