chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	44537056	44537057	A	T	24	GENIC	homozygous	139928835
16	44537064	44537075	CGGTTCTCGGC		22	GENIC	homozygous	139834495
16	44537670	44537670		T	25	GENIC	homozygous	139834496
16	44538539	44538542	AAC		17	GENIC	homozygous	139834497
16	44539160	44539161	G	A	23	GENIC	homozygous	139928839
16	44538015	44538016	A	G	24	GENIC	homozygous	139928836
16	44538079	44538080	G	A	24	GENIC	homozygous	139928837
16	44539004	44539005	A	G	20	GENIC	homozygous	139928838
16	44539449	44539450	T	C	30	GENIC	homozygous	139928840
16	44540149	44540150	A	G	19	GENIC	homozygous	139928841
16	44540883	44540884	A	T	22	GENIC	homozygous	139928842
16	44541083	44541084	G	A	21	GENIC	homozygous	139928843
16	44541753	44541753		AAAAT	23	GENIC	homozygous	139834498
16	44541808	44541809	A	G	27	GENIC	homozygous	139928844
16	44542057	44542058	C	A	23	GENIC	homozygous	139928845
16	44542463	44542464	C	T	29	GENIC	homozygous	139928846
16	44542803	44542804	G	A	19	GENIC	homozygous	139928847
16	44542822	44542823	A	G	17	GENIC	homozygous	139928848
16	44542825	44542826	A	T	17	GENIC	homozygous	139928849
16	44543138	44543139	G	A	27	GENIC	homozygous	139928850
16	44543953	44543954	G	A	22	GENIC	possibly homozygous	139928851
16	44543989	44543990	C		24	GENIC	possibly homozygous	139834499
16	44544081	44544082	C	T	32	GENIC	homozygous	139928852
16	44544228	44544229	C	T	21	GENIC	homozygous	139928853
16	44544355	44544356	G	T	14	GENIC	homozygous	139928854
16	44544738	44544738		AATC	27	GENIC	homozygous	139834500
16	44545536	44545538	CC		21	GENIC	homozygous	139834501
16	44545539	44545652	TGATTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCAACAGC		21	GENIC	homozygous	139834502
16	44545716	44545717	T	G	18	GENIC	homozygous	139928855
16	44545863	44545864	C	A	18	GENIC	homozygous	139928856
16	44545600	44545601	C		21	GENIC	homozygous	403909240
16	44545600	44545601	C	T	21	GENIC	heterozygous	403909241