chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	23120559	23120560	G	T	62	GENIC	homozygous	146449285
7	23120775	23120776	T	A	42	GENIC	homozygous	138034895
7	23121212	23121213	A	G	28	GENIC	homozygous	138034896
7	23122794	23122795	C	T	41	GENIC	homozygous	154436523
7	23122794	23122795	C		41	GENIC	heterozygous	403204353
7	23122733	23122734	A		9	GENIC	heterozygous	403204351
7	23122733	23122734	A	T	9	GENIC	possibly homozygous	403204352
7	23124274	23124275	A	T	33	GENIC	possibly homozygous	138034904
7	23125953	23125954	T	C	40	GENIC	homozygous	138034913
7	23126714	23126715	C	T	47	GENIC	homozygous	146449286
7	23127510	23127511	G	T	32	GENIC	homozygous	138034917
7	23127752	23127754	TT		44	GENIC	homozygous	137941595
7	23126808	23126808		C	39	GENIC	homozygous	137941591
7	23127373	23127373		T	49	GENIC	homozygous	137941592
7	23127375	23127375		TTGCGGGCA	50	GENIC	homozygous	137941593
7	23127962	23127963	C	T	44	GENIC	homozygous	138034919
7	23128706	23128707	C	T	43	GENIC	homozygous	146449287
7	23130254	23130255	C	T	30	GENIC	homozygous	138034932
7	23130665	23130666	T	G	39	GENIC	homozygous	138034935
7	23128248	23128256	CTAGGCTA		45	GENIC	homozygous	146435755
7	23129208	23129208		A	38	GENIC	homozygous	146435756
7	23128902	23128902		TG	8	GENIC	heterozygous	147667991