chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	83326374	83326375	C	G	25	GENIC	possibly homozygous	111881669
16	83326493	83326494	T	C	27	GENIC	homozygous	111881671
16	83327489	83327490	T	C	25	GENIC	possibly homozygous	111881675
16	83327851	83327852	A	C	19	GENIC	possibly homozygous	111881679
16	83328963	83328964	G	A	26	GENIC	homozygous	111881685
16	83329157	83329158	C	T	29	GENIC	possibly homozygous	112213342
16	83329849	83329850	G	A	35	GENIC	homozygous	111881693
16	83329856	83329857	T	C	35	GENIC	homozygous	111881695
16	83330298	83330299	A	G	20	GENIC	homozygous	111881697
16	83330379	83330380	G	A	29	GENIC	possibly homozygous	111881699
16	83330784	83330785	A	G	33	GENIC	possibly homozygous	111881705
16	83330830	83330831	A	G	33	GENIC	homozygous	111881707
16	83331535	83331536	C	T	25	GENIC	homozygous	112213344
16	83334153	83334154	T	A	32	GENIC	homozygous	111881727
16	83334687	83334688	A	G	37	GENIC	possibly homozygous	111881729
16	83340378	83340379	A	C	17	GENIC	homozygous	111881779
16	83340807	83340808	A	G	35	GENIC	possibly homozygous	111881787
16	83342510	83342511	A	C	9	GENIC	homozygous	111881803