chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	52572237	52572238	T	C	17	GENIC	possibly homozygous	51956692
9	52572687	52572688	C	T	9	GENIC	homozygous	52629047
9	52572854	52572855	G	T	12	GENIC	homozygous	51956695
9	52572903	52572904	A	G	17	GENIC	homozygous	51956698
9	52572917	52572918	G	T	17	GENIC	homozygous	51956701
9	52573120	52573121	A	G	11	GENIC	homozygous	51956704
9	52573178	52573179	T	C	9	GENIC	possibly homozygous	51956707
9	52573208	52573209	A	T	11	GENIC	possibly homozygous	51956710
9	52573234	52573235	C	A	13	GENIC	homozygous	51956713
9	52573340	52573341	T	A	14	GENIC	possibly homozygous	51956716
9	52573627	52573628	A	G	18	GENIC	homozygous	51956719
9	52573730	52573733	TAG	---	4	GENIC	homozygous	51956722
9	52573789	52573790	T	A	7	GENIC	heterozygous	51956725
9	52574192	52574193	A	G	19	GENIC	possibly homozygous	51956728
9	52574489	52574490	C	T	8	GENIC	possibly homozygous	51956734
9	52574696	52574697	T	C	9	GENIC	homozygous	51956737
9	52574737	52574738	T	C	10	GENIC	homozygous	51956740
9	52575120	52575121	G	A	16	GENIC	possibly homozygous	51956743
9	52575450	52575451	A	G	13	GENIC	homozygous	51956746
9	52575671	52575672	A	G	11	GENIC	homozygous	51956749
9	52576268	52576269	C	A	10	GENIC	heterozygous	51956752
9	52576280	52576281	T	G	9	GENIC	homozygous	51956755
9	52576321	52576322	G	C	13	GENIC	possibly homozygous	51956758
9	52576513	52576514	C	CT	7	GENIC	homozygous	51956761
9	52576610	52576611	T	C	13	GENIC	possibly homozygous	51956765
9	52576650	52576651	T	A	23	GENIC	homozygous	51956768
9	52576831	52576832	A	G	20	GENIC	possibly homozygous	51956771
9	52577012	52577013	A	T	17	GENIC	possibly homozygous	51956774
9	52577413	52577414	C	T	17	GENIC	homozygous	51956777
9	52577502	52577503	A	T	8	GENIC	homozygous	51956780
9	52577622	52577623	A	G	9	GENIC	heterozygous	51956783
9	52577656	52577657	A	G	12	GENIC	homozygous	51956786