chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	2617911	2617912	G	A	38	GENIC	homozygous	111698368
16	2619388	2619389	C	A	39	GENIC	heterozygous	119092837
16	2619568	2619569	G	A	21	GENIC	homozygous	119092838
16	2619628	2619629	C	G	39	GENIC	homozygous	111698370
16	2619675	2619676	T	A	44	GENIC	homozygous	112048352
16	2619680	2619681	C	G	42	GENIC	homozygous	119092839
16	2621744	2621745	A	G	45	GENIC	homozygous	111698372
16	2622585	2622586	T	C	33	GENIC	homozygous	119092840
16	2624815	2624816	C	A	25	GENIC	homozygous	111698374
16	2625053	2625054	G	A	18	GENIC	homozygous	111698376
16	2627276	2627277	C	G	16	GENIC	homozygous	119092841
16	2628362	2628363	G	C	53	GENIC	homozygous	111698378
16	2628854	2628855	T	C	49	GENIC	homozygous	112345486
16	2629514	2629515	G	T	34	GENIC	homozygous	119092842
16	2631873	2631874	C	A	38	GENIC	heterozygous	119092843
16	2631876	2631877	C	A	41	GENIC	heterozygous	119092844
16	2632451	2632452	A	G	72	GENIC	possibly homozygous	111698381
16	2632783	2632784	A	G	55	GENIC	possibly homozygous	111698383
16	2633097	2633098	T	C	48	GENIC	homozygous	111698385
16	2633137	2633138	C	A	48	GENIC	homozygous	111698387
16	2633161	2633162	G	C	58	GENIC	homozygous	111698389
16	2633505	2633506	A	G	37	GENIC	homozygous	111698391
16	2633760	2633761	A	G	24	GENIC	possibly homozygous	119092845
16	2634412	2634413	T	C	24	GENIC	homozygous	111698393
16	2635194	2635195	A	C	47	GENIC	homozygous	111698395