chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	129795394	129795395	A	T	21	GENIC	heterozygous	54520391
7	129796079	129796081	GT	--	19	GENIC	heterozygous	54109588
7	129796801	129796803	CC	--	9	GENIC	heterozygous	54109590
7	129798502	129798503	C	T	30	GENIC	homozygous	54520393
7	129798585	129798589	AAGC	----	18	GENIC	homozygous	54520395
7	129798843	129798844	A	C	28	GENIC	possibly homozygous	54109593
7	129799331	129799332	A	T	26	GENIC	homozygous	54520397
7	129801024	129801025	C	CT	14	GENIC	homozygous	54109595
7	129801567	129801568	G	-	24	GENIC	possibly homozygous	54109596
7	129802532	129802533	T	C	29	GENIC	homozygous	54109597
7	129803754	129803755	A	C	21	GENIC	homozygous	54109599
7	129804464	129804466	CC	--	13	GENIC	homozygous	54109601
7	129804856	129804857	C	T	21	GENIC	homozygous	54520401
7	129805274	129805275	G	A	37	GENIC	homozygous	54520403
7	129805585	129805586	C	A	35	GENIC	possibly homozygous	54589476