chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10578877	10578878	T	C	20	GENIC	homozygous	46059331
19	10579026	10579027	G	A	37	GENIC	homozygous	46279817
19	10579175	10579176	C	T	34	GENIC	homozygous	46279818
19	10580202	10580203	G	A	26	GENIC	homozygous	46279819
19	10580339	10580340	C	T	36	GENIC	homozygous	46279820
19	10580798	10580799	A	G	25	GENIC	homozygous	46279821
19	10581112	10581113	T	-	17	GENIC	possibly homozygous	46271240
19	10582521	10582522	T	A	21	GENIC	homozygous	46059332
19	10582603	10582604	A	G	21	GENIC	homozygous	46279822
19	10582797	10582798	T	C	34	GENIC	homozygous	46279823
19	10583023	10583024	T	G	26	GENIC	homozygous	46279824
19	10583100	10583101	T	G	34	GENIC	homozygous	46279825
19	10584811	10584812	C	T	34	GENIC	homozygous	46279826
19	10584907	10584908	T	C	41	GENIC	homozygous	46279827
19	10585613	10585614	C	CT	12	GENIC	homozygous	46279828
19	10586033	10586034	A	G	26	GENIC	homozygous	46279829
19	10586866	10586867	T	C	18	GENIC	homozygous	46279830
19	10587513	10587514	T	TCTGACCTAGG	17	GENIC	homozygous	46279831
19	10588308	10588309	G	A	30	GENIC	homozygous	46279832
19	10588501	10588502	C	T	40	GENIC	heterozygous	46279833
19	10588509	10588510	T	C	37	GENIC	heterozygous	46059335
19	10589553	10589554	A	G	26	GENIC	homozygous	46279835
19	10591608	10591609	G	C	36	GENIC	homozygous	46279836