chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	2069626	2069627	A	G	13	GENIC	homozygous	138483880
9	2070348	2070349	T	C	17	GENIC	homozygous	138483881
9	2070349	2070350	G	A	17	GENIC	homozygous	138483882
9	2070465	2070466	T	C	15	GENIC	homozygous	138483883
9	2070644	2070644		T	11	GENIC	homozygous	138441852
9	2070747	2070748	T	C	12	GENIC	homozygous	138483884
9	2070937	2070938	G	A	16	GENIC	homozygous	138483885
9	2070982	2070983	G	C	14	GENIC	homozygous	138483886
9	2071332	2071333	T	G	11	GENIC	possibly homozygous	138483887
9	2071413	2071414	C	A	19	GENIC	homozygous	138483888
9	2071660	2071661	C	T	14	GENIC	homozygous	138483889
9	2071669	2071670	C	T	14	GENIC	homozygous	138483890
9	2071882	2071883	T	C	22	GENIC	homozygous	138483891
9	2072173	2072173		TAAC	19	GENIC	homozygous	138441853
9	2072276	2072277	C	T	15	GENIC	homozygous	138483892
9	2072301	2072302	G	A	20	GENIC	homozygous	138483893
9	2072416	2072417	T	C	25	GENIC	homozygous	138483894
9	2073011	2073012	C	T	14	GENIC	homozygous	138483895