chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	91667950	91667951	A	G	51	GENIC	homozygous	117598310
9	91668559	91668560	T	C	44	GENIC	homozygous	117598314
9	91670733	91670734	T	C	50	GENIC	homozygous	117598324
9	91671005	91671006	T	C	42	GENIC	homozygous	117598326
9	91668336	91668337	T	C	47	GENIC	homozygous	120343507
9	91668410	91668411	G	A	44	GENIC	homozygous	120343508
9	91669232	91669233	G	A	40	GENIC	homozygous	120343509
9	91671327	91671328	A	G	39	GENIC	homozygous	120343510
9	91671330	91671331	T	C	40	GENIC	homozygous	120343511
9	91671396	91671397	G	A	37	GENIC	homozygous	120343512
9	91673061	91673062	A	C	38	GENIC	homozygous	117598336
9	91674334	91674335	A	C	33	GENIC	homozygous	117891873
9	91674712	91674713	A	G	48	GENIC	homozygous	117598346
9	91677213	91677213		A	46	GENIC	homozygous	128731455
9	91677214	91677214		GGCCATGAGAACTACATGG	47	GENIC	homozygous	128731456
9	91677333	91677334	C	A	42	GENIC	homozygous	120343514
9	91678010	91678013	ATA		42	GENIC	homozygous	128731457
9	91678141	91678142	G	A	45	GENIC	homozygous	120343515
9	91678217	91678218	A	C	35	GENIC	homozygous	117891879
9	91679866	91679867	C	T	45	GENIC	homozygous	120343516
9	91681592	91681593	T	C	38	GENIC	homozygous	120343517
9	91682179	91682180	C	T	40	GENIC	homozygous	117598358
9	91683123	91683124	G	A	49	GENIC	homozygous	117598360
9	91683221	91683222	C	T	49	GENIC	homozygous	117598362
9	91677321	91677321		T	37	GENIC	possibly homozygous	133835972