chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	55249655	55249656	C	G	47	GENIC	homozygous	46167815
19	55250514	55250515	G	C	44	GENIC	homozygous	46167816
19	55250548	55250549	T	-	37	GENIC	possibly homozygous	46167817
19	55250951	55250952	C	T	41	GENIC	homozygous	46167818
19	55251145	55251146	T	A	38	GENIC	homozygous	46167819
19	55251165	55251166	T	C	38	GENIC	homozygous	46167820
19	55251185	55251186	A	T	33	GENIC	homozygous	46167821
19	55251512	55251513	G	C	41	GENIC	homozygous	46167822
19	55251731	55251733	AG	--	35	GENIC	homozygous	46167823
19	55252265	55252266	A	G	51	GENIC	homozygous	46167824
19	55252307	55252308	T	C	46	GENIC	homozygous	46167825
19	55252472	55252473	T	C	45	GENIC	homozygous	46167826
19	55252496	55252497	G	C	55	GENIC	homozygous	46167827
19	55252961	55252962	T	TTAAA	19	GENIC	homozygous	46167828
19	55253140	55253141	G	T	35	GENIC	possibly homozygous	46167829
19	55253553	55253554	C	T	27	GENIC	homozygous	46167830
19	55254347	55254348	A	G	29	GENIC	homozygous	46167831
19	55254766	55254767	A	T	53	GENIC	homozygous	46167832
19	55255074	55255075	A	T	38	GENIC	possibly homozygous	46167833
19	55255837	55255838	C	T	23	GENIC	homozygous	46167834
19	55255945	55255947	TC	--	16	GENIC	heterozygous	46167835
19	55255976	55255980	CTAC	----	10	GENIC	homozygous	46167836
19	55256036	55256054	TGTGTGTGTGTGTGTGTA	------------------	9	GENIC	possibly homozygous	46167837
19	55257745	55257746	A	G	32	GENIC	homozygous	46167838