chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	56340288	56340289	G	T	12	GENIC	homozygous	51891801
10	56340351	56340352	T	C	8	GENIC	homozygous	51891804
10	56340804	56340805	G	A	13	GENIC	homozygous	51891807
10	56340929	56340932	AAA	---	9	GENIC	homozygous	51460059
10	56341613	56341614	C	T	7	GENIC	homozygous	51891810
10	56343229	56343230	G	A	8	GENIC	homozygous	51891819
10	56343460	56343461	C	T	8	GENIC	homozygous	51891822
10	56345487	56345488	G	A	13	INTERGENIC	homozygous	51891825
10	56345753	56345754	C	T	24	INTERGENIC	homozygous	51891828
10	56345799	56345800	T	C	22	INTERGENIC	homozygous	51891831
10	56347285	56347286	T	C	17	GENIC	homozygous	51891837
10	56347784	56347785	G	C	16	GENIC	homozygous	51654988
10	56348113	56348114	T	-	16	GENIC	homozygous	51891840
10	56348318	56348319	C	G	11	GENIC	homozygous	51891843
10	56349704	56349705	G	-	17	INTERGENIC	homozygous	51891845
10	56354405	56354406	C	G	13	INTERGENIC	homozygous	52377771
10	56354406	56354407	T	TC	13	INTERGENIC	homozygous	51891851
10	56355456	56355457	G	A	17	GENIC	homozygous	51891854
10	56356163	56356164	A	AT	10	GENIC	homozygous	51891857
10	56356395	56356396	T	TATGC	18	GENIC	homozygous	51891860
10	56356788	56356789	G	A	27	GENIC	possibly homozygous	51891863
10	56357177	56357178	A	G	17	GENIC	homozygous	51891867
10	56357836	56357837	A	G	12	GENIC	homozygous	51891873
10	56358378	56358379	A	G	13	GENIC	homozygous	51891876
10	56359674	56359675	C	T	12	GENIC	homozygous	51891881
10	56360251	56360255	TCTC	----	11	GENIC	homozygous	51891884
10	56360572	56360573	T	C	19	GENIC	homozygous	51891887
10	56360701	56360702	T	C	10	GENIC	homozygous	51891890
10	56362831	56362832	A	G	19	GENIC	homozygous	51891893
10	56362873	56362874	C	T	22	GENIC	homozygous	51891896
10	56363391	56363392	T	C	15	GENIC	homozygous	51654994
10	56364531	56364532	G	A	16	GENIC	homozygous	51654996