chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9750011	9750012	C	T	49	GENIC	homozygous	110953011
17	9750797	9750798	T	C	54	GENIC	homozygous	119263822
17	9751454	9751455	T	G	57	GENIC	homozygous	110953013
17	9752802	9752803	T	C	59	GENIC	homozygous	110953015
17	9753215	9753216	T	A	54	GENIC	homozygous	110953017
17	9756364	9756365	T	C	67	GENIC	homozygous	110953019
17	9756995	9756996	T	C	53	GENIC	homozygous	110953021
17	9758439	9758440	C	A	51	GENIC	homozygous	110953023
17	9758877	9758878	T	C	60	GENIC	homozygous	110953025
17	9759701	9759702	C	T	47	GENIC	homozygous	110953027
17	9760253	9760254	A	G	59	GENIC	homozygous	110953029
17	9754740	9754742	TG		30	GENIC	homozygous	129421280
17	9760981	9760982	T		43	GENIC	homozygous	129421283
17	9751451	9751454	ATC		57	GENIC	homozygous	129421278
17	9751709	9751710	T		33	GENIC	possibly homozygous	129421279
17	9760524	9760524		T	28	GENIC	possibly homozygous	129421281
17	9760730	9760730		A	51	GENIC	homozygous	129421282
17	9753960	9753961	G	A	32	GENIC	homozygous	111479515
17	9761051	9761052	G	A	46	GENIC	homozygous	110953031
17	9762177	9762178	T	C	50	GENIC	homozygous	110953033
17	9762414	9762415	T	A	46	GENIC	homozygous	110953035
17	9762500	9762501	C	A	48	GENIC	homozygous	110953037
17	9762557	9762558	T	C	41	GENIC	homozygous	110953039
17	9762680	9762681	A	G	52	GENIC	homozygous	110953041
17	9762691	9762692	C	T	52	GENIC	homozygous	110953043
17	9762721	9762722	T	C	57	GENIC	homozygous	110953045