chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	85344980	85344981	G	GT	23	GENIC	homozygous	52691643
8	85345685	85345686	T	TC	28	GENIC	homozygous	53000405
8	85346485	85346486	C	T	50	GENIC	homozygous	52691645
8	85346634	85346635	A	AGATG	16	GENIC	possibly homozygous	53000406
8	85347315	85347316	A	C	55	GENIC	homozygous	52691646
8	85347381	85347382	T	C	69	GENIC	homozygous	52691647
8	85348592	85348593	C	CCCTG	43	GENIC	homozygous	52691648
8	85349200	85349201	A	T	50	GENIC	homozygous	52691649
8	85350795	85350796	C	CT	45	GENIC	possibly homozygous	52691650
8	85350795	85350796	C	CTT	45	GENIC	heterozygous	53000407
8	85351467	85351468	T	C	44	GENIC	homozygous	52691651
8	85351930	85351931	A	G	77	GENIC	possibly homozygous	52691652