chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	44438884	44438889	TGCTT		22	GENIC	homozygous	129048638
13	44438935	44438935		TGACGGGAGGTGTTT	13	GENIC	homozygous	129048639
13	44439003	44439004	G	A	19	GENIC	homozygous	118449737
13	44439054	44439055	G	A	27	GENIC	homozygous	114755325
13	44442644	44442645	C	A	2	GENIC	homozygous	114334681
13	44443695	44443695		TTAGAATGATACACAGGA	45	GENIC	homozygous	129048652
13	44453349	44453350	A	G	22	GENIC	homozygous	114755327
13	44454006	44454006		C	42	GENIC	homozygous	129048653
13	44454016	44454016		TAAC	43	GENIC	possibly homozygous	129048654
13	44454049	44454050	A		38	GENIC	homozygous	129048655
13	44454096	44454097	G	A	38	GENIC	homozygous	114334683
13	44454097	44454098	A	G	39	GENIC	homozygous	114334685
13	44454115	44454117	AG		41	GENIC	homozygous	129048656
13	44454155	44454155		A	42	GENIC	homozygous	129048657
13	44454157	44454157		C	41	GENIC	homozygous	129048658
13	44454159	44454159		A	43	GENIC	homozygous	129048659
13	44454163	44454164	A	C	43	GENIC	homozygous	114755329
13	44454169	44454170	C		42	GENIC	homozygous	129048660
13	44454201	44454202	G		43	GENIC	homozygous	129048661
13	44454213	44454214	G		39	GENIC	homozygous	129048662
13	44454217	44454217		T	40	GENIC	homozygous	129048663
13	44454272	44454272		A	39	GENIC	homozygous	129048664
13	44454283	44454283		A	41	GENIC	homozygous	129048665
13	44454305	44454305		GA	35	GENIC	homozygous	129048666
13	44454343	44454343		G	38	GENIC	homozygous	129048667
13	44454366	44454366		G	35	GENIC	homozygous	129048668
13	44454420	44454420		C	39	GENIC	homozygous	129048669
13	44454449	44454450	C		42	GENIC	homozygous	129048670
13	44454451	44454452	C	A	43	GENIC	homozygous	114334687
13	44454456	44454456		T	42	GENIC	homozygous	129048671