chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	97356612	97356613	T	C	28	GENIC	homozygous	117612785
9	97357079	97357080	C	T	36	GENIC	homozygous	117612787
9	97357374	97357375	A	C	29	GENIC	homozygous	117612789
9	97359427	97359428	G	A	30	GENIC	homozygous	117612795
9	97360535	97360536	G	A	28	GENIC	homozygous	117612797
9	97360745	97360746	T	C	33	GENIC	homozygous	117612799
9	97361287	97361288	G	A	25	GENIC	homozygous	117396097
9	97361643	97361644	T	A	25	GENIC	homozygous	117612801
9	97364201	97364202	G	C	37	GENIC	homozygous	117612805
9	97366744	97366745	T	C	32	GENIC	homozygous	117612811
9	97363444	97363445	C	G	16	GENIC	heterozygous	117802150
9	97363446	97363447	C	G	16	GENIC	heterozygous	117802151
9	97366449	97366450	G	A	35	GENIC	homozygous	117810335