chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	52992075	52992076	A	T	20	GENIC	homozygous	117339686
9	52992292	52992293	G	A	14	GENIC	homozygous	128771729
9	52992582	52992582		ATCA	3	GENIC	homozygous	128711815
9	53002675	53002676	C	T	4	GENIC	homozygous	128771730
9	53002757	53002757		TGTT	10	GENIC	homozygous	128711816
9	53003078	53003079	G	A	17	GENIC	homozygous	123176433
9	53003078	53003078		A	17	GENIC	homozygous	128711817
9	53003396	53003397	C	T	28	GENIC	homozygous	117339688
9	53003403	53003404	T	A	31	GENIC	homozygous	117339689
9	53003405	53003406	C	T	31	GENIC	homozygous	117339690
9	53003717	53003718	A	T	12	GENIC	homozygous	117339693
9	53003918	53003919	T	C	22	GENIC	homozygous	117339694
9	53004752	53004753	G	T	13	GENIC	homozygous	117546076
9	53003599	53003600	G	A	28	GENIC	homozygous	117546070
9	53003603	53003604	C	T	28	GENIC	homozygous	117546072
9	53004751	53004752	A	T	13	GENIC	homozygous	117546074
9	53004987	53004988	A	G	33	GENIC	homozygous	117546078
9	53005036	53005037	C	T	31	GENIC	homozygous	117546080
9	53007230	53007231	T	G	30	GENIC	homozygous	117339699
9	53007527	53007528	T	A	23	GENIC	possibly homozygous	117546082
9	53007853	53007854	A	T	18	GENIC	homozygous	117546084
9	53007854	53007855	A	T	18	GENIC	homozygous	117546086