chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	113301365	113301366	C	T	18	GENIC	homozygous	117645062
9	113303582	113303583	A	G	40	GENIC	homozygous	117645063
9	113303899	113303900	T	C	30	GENIC	homozygous	117645064
9	113304876	113304877	A	G	32	GENIC	homozygous	117645065
9	113305312	113305313	A	C	21	GENIC	homozygous	117645066
9	113305386	113305387	A	G	36	GENIC	homozygous	117645067
9	113309222	113309223	G	A	36	GENIC	homozygous	117645068
9	113309522	113309523	A	G	25	GENIC	homozygous	117645069
9	113312922	113312923	G	A	26	GENIC	homozygous	117645070
9	113312977	113312978	G	A	28	GENIC	homozygous	117645071
9	113316649	113316650	A	G	51	GENIC	homozygous	117645072
9	113318875	113318876	C	A	14	GENIC	homozygous	117645073
9	113323569	113323570	A	C	19	GENIC	homozygous	117645074
9	113324814	113324815	A	G	43	GENIC	homozygous	117645075
9	113325461	113325462	C	G	45	GENIC	homozygous	117645076
9	113326062	113326063	A	G	50	GENIC	homozygous	117645077
9	113328505	113328506	T	G	12	GENIC	homozygous	117645078
9	113331355	113331356	C	A	7	GENIC	homozygous	117645080
9	113331727	113331728	A	C	6	GENIC	homozygous	117645081
9	113331836	113331837	C	T	9	GENIC	homozygous	117645082