chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	145118052	145118053	G	A	6	GENIC	homozygous	115946569
7	145119351	145119352	A	G	29	GENIC	homozygous	115946571
7	145120078	145120079	T	G	14	GENIC	homozygous	115946573
7	145120692	145120693	C	A	26	GENIC	possibly homozygous	115946575
7	145120839	145120840	C	T	18	GENIC	homozygous	115946577
7	145121171	145121172	T	C	27	GENIC	homozygous	115946580
7	145121810	145121811	T	G	36	GENIC	homozygous	115946582
7	145121967	145121968	G	T	32	GENIC	possibly homozygous	115946588
7	145122094	145122095	G	A	32	GENIC	homozygous	115946590
7	145123742	145123743	A	T	11	GENIC	homozygous	115946591
7	145124175	145124176	A	G	27	GENIC	homozygous	115946593
7	145124844	145124845	G	A	18	GENIC	homozygous	115946595
7	145125788	145125789	A	G	26	GENIC	homozygous	115946597
7	145125874	145125875	G	A	42	GENIC	homozygous	115946599
7	145126437	145126438	G	A	18	GENIC	homozygous	115946601
7	145128606	145128607	T	C	5	GENIC	homozygous	115946603
7	145129161	145129162	A	G	17	GENIC	homozygous	115946605
7	145130955	145130956	G	A	20	GENIC	homozygous	115946607
7	145131424	145131425	G	A	29	GENIC	possibly homozygous	115946609
7	145135727	145135728	G	A	22	GENIC	homozygous	115946613
7	145136230	145136231	G	A	30	GENIC	homozygous	115946614