chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9009251	9009252	C	T	27	GENIC	homozygous	110950880
17	9009327	9009328	T	C	30	GENIC	homozygous	110950882
17	9009528	9009529	A	G	25	GENIC	homozygous	110950884
17	9010105	9010106	C	T	24	GENIC	homozygous	110950888
17	9010184	9010185	A	G	30	GENIC	homozygous	110950890
17	9010566	9010567	G	A	29	GENIC	homozygous	110950892
17	9010986	9010987	T	C	31	GENIC	homozygous	110950894
17	9011525	9011526	T	C	34	GENIC	homozygous	110950898
17	9011775	9011776	C	T	26	GENIC	homozygous	110950900
17	9011820	9011821	C	T	26	GENIC	homozygous	110950902
17	9012040	9012041	G	A	34	GENIC	homozygous	110950904
17	9012217	9012218	C	T	30	GENIC	homozygous	110950906
17	9012233	9012234	G	T	35	GENIC	homozygous	110950908
17	9012559	9012560	T	C	26	GENIC	homozygous	110950910
17	9015340	9015341	C	T	23	GENIC	homozygous	110950912
17	9015871	9015872	G	C	20	GENIC	homozygous	111381093
17	9017559	9017560	A	G	26	GENIC	homozygous	110950914
17	9018345	9018346	G	A	32	GENIC	homozygous	110950916
17	9019216	9019217	A	T	29	GENIC	homozygous	110950918
17	9022101	9022102	C	T	33	GENIC	homozygous	110950920
17	9022236	9022237	C	T	45	GENIC	homozygous	110950922
17	9022262	9022263	A	G	46	GENIC	homozygous	110950924
17	9022678	9022679	A	G	39	GENIC	homozygous	110950926
17	9024251	9024252	T	C	33	GENIC	homozygous	110950930