chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	52166952	52166953	A	G	20	GENIC	homozygous	112508664
15	52167429	52167430	T	G	22	GENIC	homozygous	112682808
15	52167606	52167607	C	T	21	GENIC	homozygous	112508666
15	52168880	52168881	G	A	19	GENIC	homozygous	112508668
15	52169010	52169011	T	C	21	GENIC	homozygous	112508670
15	52169021	52169022	C	T	21	GENIC	homozygous	112508672
15	52169603	52169604	T	C	45	GENIC	homozygous	112508674
15	52169831	52169832	T	C	28	GENIC	possibly homozygous	112508676
15	52170603	52170604	T	C	29	GENIC	homozygous	112508678
15	52171587	52171588	C	T	18	GENIC	homozygous	112508680
15	52173487	52173488	G	A	23	GENIC	possibly homozygous	112508682
15	52174383	52174384	T	A	21	GENIC	homozygous	112508684
15	52174761	52174762	G	A	25	GENIC	homozygous	112508686
15	52175115	52175116	G	A	22	GENIC	homozygous	112508688
15	52175125	52175126	T	C	20	GENIC	homozygous	112508690
15	52175139	52175140	G	A	19	GENIC	homozygous	112508692
15	52175592	52175593	T	A	23	GENIC	homozygous	112508694
15	52176926	52176927	C	G	26	GENIC	homozygous	112508698
15	52177011	52177012	C	T	23	GENIC	homozygous	112508700
15	52177333	52177334	A	G	27	GENIC	homozygous	112682810
15	52188822	52188823	C	T	14	GENIC	homozygous	112682812
15	52202365	52202366	T	C	22	GENIC	homozygous	112508732
15	52202603	52202604	T	C	18	GENIC	homozygous	112682814
15	52203567	52203568	T	A	22	GENIC	homozygous	112682816
15	52203601	52203602	C	T	22	GENIC	possibly homozygous	112682818
15	52204452	52204453	A	C	20	GENIC	homozygous	112682820
15	52204933	52204934	G	T	24	GENIC	homozygous	112508744
15	52205787	52205788	G	A	22	GENIC	homozygous	112682822
15	52207689	52207690	T	C	23	GENIC	homozygous	112682824
15	52178461	52178462	A	G	32	GENIC	possibly homozygous	112988384
15	52204185	52204186	T	A	26	GENIC	heterozygous	119060395
15	52210094	52210095	G	C	14	GENIC	homozygous	119060396