chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	85344980	85344981	G	GT	9	GENIC	homozygous	52691643
8	85345685	85345686	T	TC	12	GENIC	homozygous	53000405
8	85346485	85346486	C	T	22	GENIC	homozygous	52691645
8	85346634	85346635	A	AGATG	9	GENIC	homozygous	53000406
8	85347315	85347316	A	C	29	GENIC	homozygous	52691646
8	85347381	85347382	T	C	35	GENIC	homozygous	52691647
8	85348592	85348593	C	CCCTG	31	GENIC	homozygous	52691648
8	85349200	85349201	A	T	38	GENIC	homozygous	52691649
8	85350795	85350796	C	CT	32	GENIC	possibly homozygous	52691650
8	85351467	85351468	T	C	13	GENIC	homozygous	52691651
8	85351930	85351931	A	G	23	GENIC	homozygous	52691652