chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	97356612	97356613	T	C	17	GENIC	homozygous	117612785
9	97357079	97357080	C	T	20	GENIC	homozygous	117612787
9	97357374	97357375	A	C	20	GENIC	homozygous	117612789
9	97358629	97358630	G	T	20	GENIC	homozygous	117612791
9	97358869	97358870	G	A	24	GENIC	homozygous	117612793
9	97359427	97359428	G	A	25	GENIC	homozygous	117612795
9	97360535	97360536	G	A	23	GENIC	homozygous	117612797
9	97360745	97360746	T	C	25	GENIC	homozygous	117612799
9	97361287	97361288	G	A	21	GENIC	homozygous	117396097
9	97361643	97361644	T	A	25	GENIC	homozygous	117612801
9	97363927	97363928	T	C	21	GENIC	homozygous	117612803
9	97364201	97364202	G	C	22	GENIC	homozygous	117612805
9	97364476	97364477	A	G	22	GENIC	homozygous	117612807
9	97365314	97365315	A	G	18	GENIC	possibly homozygous	117612809
9	97366744	97366745	T	C	34	GENIC	possibly homozygous	117612811