chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	54000915	54000916	G	A	13	GENIC	homozygous	111825513
16	54002581	54002582	A	G	28	GENIC	homozygous	111825515
16	54003521	54003522	A	C	31	GENIC	homozygous	111825517
16	54003809	54003810	C	T	34	GENIC	homozygous	111985069
16	54007267	54007268	T	C	47	GENIC	possibly homozygous	111825519
16	54008263	54008264	G	A	89	GENIC	heterozygous	119119182
16	54008269	54008270	A	G	85	GENIC	heterozygous	119119183
16	54009173	54009174	C	A	27	GENIC	homozygous	111825521
16	54011125	54011126	A	G	59	GENIC	possibly homozygous	111825523
16	54013150	54013151	A	G	34	GENIC	possibly homozygous	119119184
16	54013702	54013703	T	A	65	GENIC	homozygous	111825525
16	54015247	54015248	T	C	53	GENIC	homozygous	111825527
16	54015556	54015557	A	G	33	GENIC	homozygous	111825529
16	54018226	54018227	A	G	35	GENIC	possibly homozygous	111825531
16	54023661	54023662	T	C	56	GENIC	homozygous	111825533
16	54025048	54025049	A	C	17	GENIC	homozygous	111825535
16	54026394	54026395	T	G	24	GENIC	homozygous	111825537
16	54026464	54026465	C	T	35	GENIC	possibly homozygous	111825539
16	54026468	54026469	A	G	33	GENIC	homozygous	111825541
16	54028001	54028002	G	A	46	GENIC	homozygous	111825543
16	54028415	54028416	T	C	48	GENIC	homozygous	111825545
16	54028517	54028518	C	T	61	GENIC	possibly homozygous	111825547
16	54029669	54029670	C	T	36	GENIC	homozygous	112435625
16	54029705	54029706	C	T	35	GENIC	homozygous	111825549