chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	30068987	30068988	A	G	66	GENIC	heterozygous	117302956
9	30069121	30069122	G	A	89	GENIC	heterozygous	117302957
9	30069408	30069409	T	C	65	GENIC	heterozygous	117302958
9	30072135	30072136	T	C	68	GENIC	heterozygous	117302966
9	30114312	30114313	A	T	36	GENIC	homozygous	117303106
9	30114348	30114349	C	A	3	GENIC	homozygous	117491952
9	30114377	30114378	C	T	45	GENIC	homozygous	117303107
9	30114400	30114401	C	G	46	GENIC	homozygous	117303108
9	30114431	30114432	G	A	32	GENIC	homozygous	117303109
9	30114454	30114455	T	G	32	GENIC	homozygous	117303110
9	30114460	30114461	G	A	32	GENIC	homozygous	117303111
9	30114794	30114795	A	T	52	GENIC	possibly homozygous	117303114
9	30115119	30115120	C	T	3	GENIC	homozygous	117303118
9	30115225	30115226	A	C	18	GENIC	homozygous	117303120
9	30133688	30133689	A	G	94	GENIC	heterozygous	117303185
9	30133806	30133807	C	T	65	GENIC	heterozygous	117303186
9	30133825	30133826	C	T	62	GENIC	heterozygous	117303187
9	30133847	30133848	A	G	67	GENIC	heterozygous	117303188
9	30134183	30134184	C	G	58	GENIC	heterozygous	117303189
9	30134308	30134309	A	G	33	GENIC	heterozygous	117303190
9	30161740	30161741	A	C	12	GENIC	homozygous	117303296