chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	85344980	85344981	G	GT	7	GENIC	homozygous	52691643
8	85345531	85345532	C	-	18	GENIC	heterozygous	53324630
8	85345686	85345687	C	-	14	GENIC	heterozygous	52691644
8	85345878	85345879	G	T	19	GENIC	heterozygous	53324631
8	85346024	85346025	G	-	12	GENIC	heterozygous	53324632
8	85346026	85346028	TG	--	12	GENIC	heterozygous	53324633
8	85346485	85346486	C	T	9	GENIC	heterozygous	52691645
8	85347315	85347316	A	C	17	GENIC	homozygous	52691646
8	85347321	85347322	G	A	17	GENIC	heterozygous	53324635
8	85347381	85347382	T	C	10	GENIC	homozygous	52691647
8	85347532	85347533	G	C	16	GENIC	heterozygous	53324636
8	85348360	85348361	T	TGGTTC	8	GENIC	homozygous	53324638
8	85348592	85348593	C	CCCTG	20	GENIC	homozygous	52691648
8	85348934	85348935	C	T	14	GENIC	heterozygous	53324640
8	85349200	85349201	A	T	17	GENIC	homozygous	52691649
8	85350094	85350095	A	G	10	GENIC	heterozygous	53324641
8	85350201	85350202	A	G	12	GENIC	heterozygous	53324642
8	85350592	85350593	A	G	21	GENIC	heterozygous	53324643
8	85350612	85350613	G	A	23	GENIC	heterozygous	53324644
8	85352489	85352490	A	G	8	GENIC	homozygous	52691653
8	85352593	85352594	C	A	10	GENIC	heterozygous	53324653
8	85352750	85352751	G	A	6	GENIC	heterozygous	53324654