chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	16528995	16528996	C	T	25	GENIC	homozygous	117269422
9	16529098	16529099	A	G	30	GENIC	homozygous	117269423
9	16529126	16529127	T	C	31	GENIC	homozygous	117269424
9	16529317	16529318	A	G	45	GENIC	homozygous	117269426
9	16529388	16529389	T	G	27	GENIC	homozygous	117269427
9	16529708	16529709	A	G	36	GENIC	homozygous	117269428
9	16529873	16529874	C	T	19	GENIC	homozygous	117681348
9	16530105	16530106	C	T	33	GENIC	homozygous	117269430
9	16530502	16530503	G	A	27	GENIC	homozygous	117269433
9	16530745	16530746	T	C	42	GENIC	possibly homozygous	117269434
9	16531351	16531352	G	A	42	GENIC	homozygous	117681350
9	16531684	16531685	C	T	41	GENIC	homozygous	117681352
9	16532532	16532533	A	C	17	GENIC	homozygous	117269443
9	16533326	16533327	C	A	25	GENIC	homozygous	117269445
9	16533400	16533401	A	G	27	GENIC	homozygous	117681356
9	16533718	16533719	C	T	23	GENIC	homozygous	117681358
9	16534358	16534359	C	T	23	GENIC	possibly homozygous	117681360
9	16535100	16535101	C	T	16	GENIC	possibly homozygous	117681362
9	16535530	16535531	C	A	25	GENIC	homozygous	117269453
9	16535589	16535590	C	T	19	GENIC	homozygous	117674080
9	16536183	16536184	T	G	36	GENIC	homozygous	117269458
9	16536194	16536195	G	A	37	GENIC	homozygous	117681364
9	16538122	16538123	G	A	41	GENIC	homozygous	117681366
9	16538860	16538861	C	T	30	GENIC	homozygous	117681368