chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	73257356	73257357	G	A	12	GENIC	homozygous	122799547
7	73258866	73258867	T	C	4	GENIC	homozygous	116036872
7	73259247	73259248	T	A	4	GENIC	heterozygous	116036876
7	73259860	73259861	A	G	9	GENIC	homozygous	116036878
7	73259912	73259913	G	A	10	GENIC	homozygous	122799552
7	73260279	73260280	A	G	28	GENIC	homozygous	116036884
7	73260471	73260472	C	T	6	GENIC	homozygous	116036888
7	73260596	73260597	C	G	23	GENIC	homozygous	116036890
7	73261435	73261436	T	C	9	GENIC	homozygous	116036894
7	73261663	73261664	G	A	17	GENIC	homozygous	122799557
7	73261698	73261699	C	T	20	GENIC	possibly homozygous	116036898
7	73262265	73262266	G	A	19	GENIC	homozygous	116036900
7	73262327	73262328	A	G	8	GENIC	homozygous	122799558
7	73264506	73264507	A	G	19	GENIC	homozygous	115714063
7	73265141	73265142	C	T	9	GENIC	homozygous	115714066
7	73264870	73264871	T	C	14	GENIC	homozygous	126631955
7	73267068	73267069	T	C	10	GENIC	homozygous	115714073
7	73267370	73267371	C	T	9	GENIC	homozygous	116036920
7	73268574	73268575	G	C	20	GENIC	homozygous	115714078
7	73269508	73269509	T	G	24	GENIC	homozygous	122799567