chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53504902	53504903	A	T	29	GENIC	homozygous	116887042
10	53505066	53505067	T	C	20	GENIC	homozygous	116887044
10	53505071	53505072	A	T	19	GENIC	homozygous	116887046
10	53505707	53505708	C	T	20	GENIC	homozygous	116887048
10	53505999	53506000	G	A	21	GENIC	homozygous	116887050
10	53506325	53506326	A	G	31	GENIC	homozygous	118103344
10	53506478	53506479	A	G	25	GENIC	homozygous	117011000
10	53507185	53507186	A	G	23	GENIC	homozygous	116887060
10	53508192	53508193	C	G	25	GENIC	homozygous	116887062
10	53508320	53508321	C	T	27	GENIC	homozygous	117195761
10	53508442	53508443	C	A	13	GENIC	homozygous	118103346
10	53508878	53508879	A	T	22	GENIC	homozygous	116887070
10	53510218	53510219	T	C	28	GENIC	possibly homozygous	117195763
10	53510594	53510595	C	T	19	GENIC	homozygous	117195764
10	53510690	53510691	T	C	23	GENIC	homozygous	116887072
10	53510916	53510917	A	C	19	GENIC	homozygous	116887076
10	53510919	53510920	A	C	21	GENIC	possibly homozygous	117195765
10	53510939	53510940	T	C	17	GENIC	homozygous	116887078
10	53510969	53510970	G	C	18	GENIC	homozygous	116887080
10	53510972	53510973	T	G	17	GENIC	homozygous	116887082
10	53510978	53510979	A	G	16	GENIC	homozygous	116887084
10	53511028	53511029	T	C	15	GENIC	homozygous	116887086
10	53511479	53511480	G	A	11	GENIC	homozygous	117195766
10	53511859	53511860	A	G	28	GENIC	homozygous	116887088
10	53511977	53511978	G	A	20	GENIC	homozygous	117195767
10	53512213	53512214	T	C	22	GENIC	homozygous	116887092
10	53512726	53512727	A	G	21	GENIC	homozygous	116887098
10	53512942	53512943	G	A	27	GENIC	homozygous	116887100
10	53512953	53512954	T	C	25	GENIC	homozygous	116887104