chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102136316	102136317	G	-	23	GENIC	possibly homozygous	51587352
10	102137007	102137008	T	C	24	GENIC	homozygous	51587354
10	102137511	102137512	A	G	35	GENIC	homozygous	51587356
10	102137788	102137789	G	A	23	GENIC	homozygous	51587358
10	102137857	102137858	T	C	21	GENIC	homozygous	51587360
10	102137865	102137866	A	G	19	GENIC	homozygous	51587362
10	102138327	102138328	A	G	14	GENIC	homozygous	51587364
10	102139127	102139128	G	A	25	GENIC	possibly homozygous	51587366
10	102139449	102139450	T	C	26	GENIC	homozygous	51587368
10	102139634	102139635	A	T	23	GENIC	homozygous	51587370
10	102139666	102139669	TTC	---	21	GENIC	homozygous	51587374
10	102139770	102139771	C	T	13	GENIC	homozygous	51587376
10	102140038	102140039	C	T	23	GENIC	homozygous	51587378
10	102140142	102140143	C	CACACAGAG	8	GENIC	possibly homozygous	52403770
10	102140142	102140143	C	CAG	8	GENIC	heterozygous	52447271
10	102140505	102140506	T	C	13	GENIC	homozygous	51587380
10	102141647	102141648	A	G	23	GENIC	homozygous	51587382
10	102141652	102141653	A	G	23	GENIC	homozygous	51587384
10	102141692	102141693	C	A	30	GENIC	homozygous	51587386
10	102141972	102141973	T	-	20	GENIC	homozygous	51587388
10	102142112	102142113	T	TG	26	GENIC	homozygous	51587390
10	102142276	102142277	T	C	26	GENIC	homozygous	51587392
10	102143189	102143190	C	CAAA	9	GENIC	possibly homozygous	51587396