chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89253765	89253766	A	G	23	GENIC	homozygous	51536901
10	89253875	89253876	A	G	16	GENIC	homozygous	51925725
10	89254171	89254172	A	-	4	GENIC	homozygous	51536902
10	89254710	89254711	C	T	16	GENIC	homozygous	51536903
10	89255547	89255548	A	G	1	GENIC	homozygous	51925729
10	89255802	89255803	C	T	12	GENIC	heterozygous	51925731
10	89255805	89255806	G	C	8	GENIC	possibly homozygous	51925733
10	89256441	89256442	C	T	6	GENIC	heterozygous	51925735
10	89257091	89257093	CC	--	3	GENIC	heterozygous	51732552
10	89258501	89258502	G	A	18	GENIC	possibly homozygous	51925739
10	89262963	89262964	T	-	19	GENIC	possibly homozygous	51536919
10	89263363	89263480	AAAACCTAAACTCTGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAGTCCAAAAAAAAAAAA	---------------------------------------------------------------------------------------------------------------------	15	GENIC	possibly homozygous	52323045
10	89265688	89265689	G	A	10	GENIC	homozygous	51925741
10	89268260	89268262	TC	--	6	GENIC	homozygous	51925743
10	89269425	89269426	T	C	20	GENIC	possibly homozygous	51536933
10	89269765	89269766	C	T	14	GENIC	homozygous	51925745
10	89273165	89273166	T	C	5	GENIC	homozygous	51536940
10	89275636	89275637	A	G	12	GENIC	homozygous	51536945
10	89276218	89276220	AA	--	1	GENIC	homozygous	51732604
10	89278833	89278834	T	C	19	GENIC	possibly homozygous	51536956
10	89278972	89278973	T	A	11	GENIC	possibly homozygous	51925749
10	89279196	89279197	G	A	28	GENIC	homozygous	51925751
10	89279707	89279708	A	G	14	GENIC	homozygous	51536960
10	89279869	89279870	G	A	10	GENIC	possibly homozygous	51925753
10	89281661	89281662	T	C	9	GENIC	heterozygous	51536965