chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10676962	10676963	A	G	10	GENIC	homozygous	110954825
17	10677252	10677253	T	C	9	GENIC	homozygous	110954827
17	10677506	10677507	G	A	11	GENIC	homozygous	110954829
17	10678066	10678067	G	A	16	GENIC	homozygous	110954831
17	10678603	10678604	C	T	23	GENIC	homozygous	110954833
17	10678608	10678609	G	A	23	GENIC	homozygous	110954835
17	10679167	10679168	A	G	13	GENIC	homozygous	110954837
17	10679636	10679637	A	T	7	GENIC	homozygous	110954839
17	10680171	10680172	T	G	23	GENIC	homozygous	111295113
17	10680275	10680276	C	T	29	GENIC	homozygous	110954841
17	10680335	10680336	G	A	27	GENIC	homozygous	110954843
17	10680393	10680394	C	G	17	GENIC	homozygous	110954845
17	10680394	10680395	A	G	17	GENIC	homozygous	110954847
17	10680450	10680451	C	T	20	GENIC	homozygous	111231063
17	10680863	10680864	A	G	16	GENIC	homozygous	110954849
17	10682455	10682456	G	A	15	GENIC	homozygous	110954851
17	10683480	10683481	A	G	9	GENIC	homozygous	110954853
17	10683977	10683978	T	C	23	GENIC	homozygous	110954856
17	10685140	10685141	A	C	9	GENIC	homozygous	110954858