chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	86053685	86053686	G	C	24	GENIC	heterozygous	47706123
16	86053692	86053693	A	C	24	GENIC	heterozygous	47777694
16	86062822	86062823	T	-	34	GENIC	heterozygous	47792152
16	86062892	86062893	G	A	53	GENIC	heterozygous	47581668
16	86062896	86062897	A	G	49	GENIC	heterozygous	47824089
16	86064260	86064261	T	TTG	24	GENIC	possibly homozygous	47581674
16	86064814	86064815	T	G	42	GENIC	heterozygous	47581675
16	86069955	86069956	A	C	52	GENIC	homozygous	47581689
16	86073405	86073407	TG	--	4	GENIC	heterozygous	47581696
16	86073479	86073480	T	C	43	GENIC	possibly homozygous	47853510
16	86062884	86062885	A	G	52	GENIC	heterozygous	47898580
16	86069862	86069863	A	G	49	GENIC	possibly homozygous	47853506
16	86070208	86070209	A	G	36	GENIC	homozygous	47853507
16	86071710	86071711	C	T	39	GENIC	homozygous	47853508
16	86072213	86072214	G	A	37	GENIC	homozygous	47853509
16	86074067	86074068	C	T	66	GENIC	homozygous	47853511
16	86074286	86074287	A	G	38	GENIC	homozygous	47581700
16	86074845	86074846	A	T	37	GENIC	homozygous	47853512
16	86074875	86074876	A	G	38	GENIC	homozygous	47581707
16	86075328	86075329	T	C	59	GENIC	homozygous	47581711
16	86079944	86079945	A	G	20	GENIC	homozygous	47581723
16	86079947	86079948	T	G	19	GENIC	homozygous	47581724
16	86079987	86079988	C	-	32	GENIC	heterozygous	47581725
16	86080623	86080624	T	TC	41	GENIC	homozygous	47853513
16	86083812	86083814	CC	--	27	GENIC	homozygous	47853514
16	86084468	86084469	G	GT	37	GENIC	possibly homozygous	47706125
16	86084739	86084740	C	G	45	GENIC	homozygous	47853515