chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	14306828	14306829	G	A	36	GENIC	possibly homozygous	112147057
16	14307449	14307450	G	A	50	GENIC	homozygous	112289680
16	14308314	14308315	A	G	25	GENIC	homozygous	111732776
16	14309493	14309494	A	G	20	GENIC	possibly homozygous	111732778
16	14309642	14309643	C	T	31	GENIC	homozygous	111732780
16	14309886	14309887	C	T	35	GENIC	homozygous	112289682
16	14310163	14310164	T	C	30	GENIC	homozygous	111732782
16	14310404	14310405	C	T	30	GENIC	homozygous	112289686
16	14310405	14310406	C	G	30	GENIC	homozygous	112289688
16	14311318	14311319	G	A	18	GENIC	homozygous	111732786
16	14311408	14311409	C	T	18	GENIC	homozygous	111732788
16	14311484	14311485	C	G	22	GENIC	homozygous	111732790
16	14311523	14311524	C	T	23	GENIC	homozygous	111732792
16	14311222	14311223	G	A	25	GENIC	homozygous	111939820
16	14312077	14312078	C	G	37	GENIC	homozygous	111732794
16	14312388	14312389	G	A	38	GENIC	homozygous	112289690
16	14312810	14312811	C	T	46	GENIC	homozygous	111732807
16	14312821	14312822	C	T	41	GENIC	homozygous	111732809
16	14312843	14312844	T	C	36	GENIC	homozygous	111732811
16	14313053	14313054	C	G	39	GENIC	homozygous	112289692
16	14313588	14313589	A	G	31	GENIC	homozygous	112147112
16	14313972	14313973	C	T	30	GENIC	homozygous	111732815