chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	81589150	81589150		C	39	GENIC	homozygous	128727755
9	81589265	81589266	T	G	33	GENIC	heterozygous	117380953
9	81598405	81598406	A		34	GENIC	homozygous	128727756
9	81598408	81598409	A		34	GENIC	homozygous	128727757
9	81605409	81605409		AACTCCCTCACAAACCTGCCCAGAGCTTCATCTCCTAATTAATTTTAGGTCCTGTTAAACTGAAAGTCAATATCAAGCATCACAAGGACAGCGAAGAGGCAAATGGTGCTTCTGATGTGAGACTTGTATGGTCAGCTTTGGACACATAGTGTGGAAAAGCTCCCAGAGCAGCTACT	59	GENIC	possibly homozygous	128727758
9	81608944	81608945	A		50	GENIC	homozygous	128727759
9	81621946	81621947	C		17	GENIC	homozygous	128727760
9	81622021	81622021		T	21	GENIC	homozygous	128727761
9	81622077	81622077		GT	41	GENIC	homozygous	128727762
9	81622113	81622114	C		44	GENIC	homozygous	128727763
9	81622229	81622230	G		40	GENIC	homozygous	128727764
9	81622268	81622271	CCC		41	GENIC	homozygous	128727765
9	81622310	81622310		C	43	GENIC	homozygous	128727766
9	81621919	81621925	TCTTCT		20	GENIC	heterozygous	130379773
9	81621989	81622003	CCTCTCTTCTCCTC		17	GENIC	homozygous	130379774
9	81622012	81622013	T		17	GENIC	homozygous	130379775
9	81621948	81621949	C	T	16	GENIC	heterozygous	130388007
9	81622144	81622145	T	C	41	GENIC	homozygous	117594225