chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	97356419	97356420	A		20	GENIC	homozygous	128735575
9	97356612	97356613	T	C	15	GENIC	homozygous	117612785
9	97357079	97357080	C	T	19	GENIC	homozygous	117612787
9	97357374	97357375	A	C	18	GENIC	homozygous	117612789
9	97359516	97359517	C	T	17	GENIC	homozygous	117785203
9	97360201	97360202	G	A	12	GENIC	homozygous	117785204
9	97360687	97360688	C	T	20	GENIC	homozygous	117785205
9	97360745	97360746	T	C	14	GENIC	homozygous	117612799
9	97361287	97361288	G	A	9	GENIC	homozygous	117396097
9	97361643	97361644	T	A	12	GENIC	homozygous	117612801
9	97362728	97362729	A	T	27	GENIC	homozygous	117785206
9	97363927	97363928	T	C	16	GENIC	homozygous	117612803
9	97364201	97364202	G	C	13	GENIC	homozygous	117612805
9	97364476	97364477	A	G	17	GENIC	homozygous	117612807
9	97364983	97364988	CATGG		22	GENIC	homozygous	128735577
9	97365314	97365315	A	G	24	GENIC	homozygous	117612809
9	97366744	97366745	T	C	15	GENIC	homozygous	117612811
9	97367405	97367406	C	T	18	GENIC	homozygous	117612813