chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	81689756	81689757	T	C	36	GENIC	homozygous	111877758
16	81690499	81690500	C	T	53	GENIC	possibly homozygous	111877760
16	81693549	81693550	C	T	46	GENIC	homozygous	111877762
16	81695382	81695383	C	G	39	GENIC	homozygous	111877764
16	81697824	81697825	G	A	40	GENIC	homozygous	111877766
16	81700668	81700669	T	A	49	GENIC	homozygous	111877768
16	81701308	81701309	T	C	44	GENIC	homozygous	111877770
16	81703039	81703040	A	G	37	GENIC	homozygous	111877772
16	81704421	81704422	C	T	54	GENIC	homozygous	111877774
16	81704668	81704669	A	G	33	GENIC	homozygous	111877776
16	81706893	81706894	C	T	51	GENIC	homozygous	111877778
16	81706975	81706976	T	C	52	GENIC	homozygous	111877780
16	81707041	81707042	C	T	43	GENIC	homozygous	111877782
16	81709120	81709121	C	T	34	GENIC	homozygous	111877784
16	81709140	81709141	C	T	40	GENIC	homozygous	111877786
16	81709393	81709394	C	T	43	GENIC	homozygous	111877788
16	81709655	81709656	T	G	34	GENIC	homozygous	111877790
16	81711434	81711435	A	G	35	GENIC	homozygous	111877792
16	81712408	81712409	A	C	42	GENIC	homozygous	111877794
16	81712431	81712432	T	C	41	GENIC	homozygous	111877796
16	81712455	81712456	A	G	40	GENIC	homozygous	111877798
16	81713531	81713532	A	T	55	GENIC	homozygous	111877800
16	81714250	81714251	T	C	67	GENIC	homozygous	111877802