chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	83326374	83326375	C	G	43	GENIC	homozygous	111881669
16	83326493	83326494	T	C	39	GENIC	homozygous	111881671
16	83326658	83326659	G	A	23	GENIC	homozygous	119134949
16	83327489	83327490	T	C	30	GENIC	homozygous	111881675
16	83327851	83327852	A	C	48	GENIC	homozygous	111881679
16	83328963	83328964	G	A	30	GENIC	homozygous	111881685
16	83329157	83329158	C	T	29	GENIC	homozygous	112213342
16	83329849	83329850	G	A	44	GENIC	homozygous	111881693
16	83329856	83329857	T	C	42	GENIC	homozygous	111881695
16	83330298	83330299	A	G	32	GENIC	homozygous	111881697
16	83330379	83330380	G	A	26	GENIC	homozygous	111881699
16	83330784	83330785	A	G	48	GENIC	homozygous	111881705
16	83330830	83330831	A	G	52	GENIC	homozygous	111881707
16	83331535	83331536	C	T	42	GENIC	homozygous	112213344
16	83334153	83334154	T	A	41	GENIC	homozygous	111881727
16	83334687	83334688	A	G	43	GENIC	possibly homozygous	111881729
16	83336954	83336955	T	G	27	GENIC	possibly homozygous	119134952
16	83340378	83340379	A	C	34	GENIC	homozygous	111881779
16	83340807	83340808	A	G	34	GENIC	homozygous	111881787
16	83341324	83341325	C	T	50	GENIC	homozygous	112213346
16	83342510	83342511	A	C	17	GENIC	homozygous	111881803
16	83337119	83337120	G	T	38	GENIC	heterozygous	119176047
16	83337203	83337204	G	T	38	GENIC	heterozygous	119176049
16	83339774	83339775	A	G	22	GENIC	heterozygous	119176051