chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10676962	10676963	A	G	6	GENIC	homozygous	110954825
17	10678066	10678067	G	A	19	GENIC	homozygous	110954831
17	10678603	10678604	C	T	30	GENIC	homozygous	110954833
17	10678608	10678609	G	A	31	GENIC	homozygous	110954835
17	10679167	10679168	A	G	23	GENIC	homozygous	110954837
17	10679636	10679637	A	T	18	GENIC	possibly homozygous	110954839
17	10680275	10680276	C	T	37	GENIC	homozygous	110954841
17	10680335	10680336	G	A	25	GENIC	homozygous	110954843
17	10680393	10680394	C	G	23	GENIC	homozygous	110954845
17	10680394	10680395	A	G	23	GENIC	homozygous	110954847
17	10680450	10680451	C	T	27	GENIC	homozygous	111231063
17	10680863	10680864	A	G	33	GENIC	homozygous	110954849
17	10682455	10682456	G	A	16	GENIC	homozygous	110954851
17	10683480	10683481	A	G	20	GENIC	homozygous	110954853
17	10683977	10683978	T	C	23	GENIC	homozygous	110954856
17	10685140	10685141	A	C	12	GENIC	homozygous	110954858