chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	90800212	90800213	A		21	GENIC	homozygous	138473765
9	90800405	90800406	T	C	16	GENIC	homozygous	138626538
9	90800870	90800871	C	T	17	GENIC	homozygous	138626539
9	90801165	90801166	A	C	14	GENIC	homozygous	138626540
9	90802420	90802421	G	T	13	GENIC	homozygous	138626541
9	90802660	90802661	G	A	18	GENIC	homozygous	138626542
9	90803218	90803219	G	A	12	GENIC	homozygous	138626543
9	90804326	90804327	G	A	17	GENIC	homozygous	138626544
9	90804536	90804537	T	C	20	GENIC	homozygous	138626545
9	90805434	90805435	T	A	19	GENIC	homozygous	138626546
9	90807718	90807719	T	C	19	GENIC	homozygous	138626547
9	90807992	90807993	G	C	20	GENIC	homozygous	138626548
9	90808086	90808087	C		23	GENIC	homozygous	138473766
9	90808267	90808268	A	G	13	GENIC	homozygous	138626549
9	90808774	90808779	CATGG		19	GENIC	homozygous	138473767
9	90809105	90809106	A	G	19	GENIC	homozygous	138626550
9	90810535	90810536	T	C	22	GENIC	homozygous	138626551
9	90811196	90811197	C	T	17	GENIC	homozygous	138626552