chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123006322	123006323	A	G	14	GENIC	possibly homozygous	54088929
7	123006866	123006867	C	T	10	GENIC	homozygous	54088932
7	123007096	123007097	C	CTT	2	GENIC	homozygous	54088933
7	123007581	123007582	A	-	24	GENIC	homozygous	54088934
7	123007910	123007911	C	T	1	GENIC	homozygous	54088935
7	123007955	123007956	A	-	1	GENIC	homozygous	54235771
7	123008068	123008069	A	G	1	GENIC	homozygous	54088940
7	123008210	123008211	G	A	6	GENIC	homozygous	54088941
7	123008288	123008289	A	G	17	GENIC	homozygous	54088942
7	123008851	123008852	C	-	6	GENIC	homozygous	54088943
7	123011831	123011832	A	C	18	GENIC	heterozygous	54088944
7	123017333	123017334	A	G	7	GENIC	homozygous	56063646
7	123020846	123020847	G	A	18	GENIC	homozygous	54088950
7	123021593	123021594	G	A	16	GENIC	possibly homozygous	54088951
7	123025959	123025960	G	C	13	GENIC	possibly homozygous	54088952
7	123026879	123026880	T	G	13	GENIC	homozygous	54088956
7	123027215	123027217	TG	--	6	GENIC	heterozygous	54088958
7	123027425	123027426	T	-	2	GENIC	heterozygous	54088959
7	123027529	123027530	A	G	15	GENIC	homozygous	54088960
7	123033013	123033014	T	C	14	GENIC	homozygous	54088961