chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	23120559	23120560	G	T	26	GENIC	homozygous	146449285
7	23120775	23120776	T	A	21	GENIC	homozygous	138034895
7	23121212	23121213	A	G	15	GENIC	homozygous	138034896
7	23122794	23122795	C	T	17	GENIC	homozygous	154436523
7	23122794	23122795	C		17	GENIC	heterozygous	403204353
7	23124274	23124275	A	T	13	GENIC	homozygous	138034904
7	23125953	23125954	T	C	15	GENIC	homozygous	138034913
7	23126714	23126715	C	T	15	GENIC	homozygous	146449286
7	23127510	23127511	G	T	15	GENIC	homozygous	138034917
7	23129208	23129208		A	15	GENIC	homozygous	146435756
7	23126808	23126808		C	27	GENIC	homozygous	137941591
7	23127373	23127373		T	17	GENIC	homozygous	137941592
7	23127375	23127375		TTGCGGGCA	16	GENIC	homozygous	137941593
7	23127752	23127754	TT		15	GENIC	homozygous	137941595
7	23128248	23128256	CTAGGCTA		17	GENIC	homozygous	146435755
7	23127962	23127963	C	T	22	GENIC	homozygous	138034919
7	23128706	23128707	C	T	8	GENIC	homozygous	146449287
7	23125387	23125388	C	T	22	GENIC	homozygous	148020003
7	23130254	23130255	C	T	16	GENIC	homozygous	138034932
7	23130665	23130666	T	G	20	GENIC	homozygous	138034935