chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9680692	9680692		GAAGTCTCAGGGTTGTCAG	27	GENIC	homozygous	129421246
17	9680766	9680767	C	A	32	GENIC	homozygous	110952867
17	9680841	9680842	A	G	41	GENIC	homozygous	111166906
17	9681321	9681322	A	G	43	GENIC	homozygous	110952869
17	9682195	9682196	T	C	39	GENIC	homozygous	110952871
17	9682195	9682195		A	39	GENIC	homozygous	129421247
17	9683037	9683037		CC	31	GENIC	homozygous	129421248
17	9683081	9683082	T		36	GENIC	homozygous	129421249
17	9684335	9684335		AGAG	54	GENIC	possibly homozygous	129421250
17	9684567	9684568	T	C	53	GENIC	homozygous	110952873
17	9685519	9685519		GAGTACTA	61	GENIC	homozygous	129421251
17	9686311	9686312	A	C	46	GENIC	possibly homozygous	110952875
17	9686367	9686368	A	G	49	GENIC	possibly homozygous	110952877
17	9686463	9686464	C	A	50	GENIC	possibly homozygous	110952879
17	9686533	9686534	G	A	45	GENIC	homozygous	110952881
17	9687376	9687377	A	G	55	GENIC	homozygous	110952883
17	9687575	9687575		TTT	50	GENIC	possibly homozygous	129421252
17	9687576	9687576		T	47	GENIC	possibly homozygous	129421253
17	9687581	9687581		TTC	47	GENIC	possibly homozygous	129421254
17	9688450	9688451	C	T	51	GENIC	homozygous	110952885
17	9688676	9688677	C	T	63	GENIC	homozygous	110952887
17	9691525	9691526	C	T	72	GENIC	homozygous	110952891