chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123006322	123006323	A	G	16	GENIC	homozygous	54088929
7	123006866	123006867	C	T	16	GENIC	homozygous	54088932
7	123007096	123007097	C	CTT	18	GENIC	homozygous	54088933
7	123007581	123007582	A	-	12	GENIC	homozygous	54088934
7	123007910	123007911	C	T	10	GENIC	homozygous	54088935
7	123008012	123008013	A	AAT	13	GENIC	homozygous	54088936
7	123008048	123008050	AT	--	14	GENIC	homozygous	54088937
7	123008060	123008061	A	G	16	GENIC	homozygous	54235773
7	123008068	123008069	A	G	15	GENIC	homozygous	54088940
7	123008210	123008211	G	A	10	GENIC	homozygous	54088941
7	123008288	123008289	A	G	12	GENIC	homozygous	54088942
7	123008851	123008852	C	-	20	GENIC	homozygous	54088943
7	123011831	123011832	A	C	16	GENIC	homozygous	54088944
7	123016222	123016223	A	-	11	GENIC	homozygous	54088948
7	123020846	123020847	G	A	16	GENIC	homozygous	54088950
7	123021593	123021594	G	A	16	GENIC	homozygous	54088951
7	123025959	123025960	G	C	18	GENIC	homozygous	54088952
7	123026879	123026880	T	G	15	GENIC	homozygous	54088956
7	123027425	123027426	T	-	8	GENIC	homozygous	54088959
7	123027529	123027530	A	G	8	GENIC	homozygous	54088960
7	123033013	123033014	T	C	22	GENIC	homozygous	54088961