chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	91834891	91834892	C	T	8	GENIC	homozygous	54021791
7	91835502	91835503	T	C	13	GENIC	homozygous	54021793
7	91835752	91835753	G	A	14	GENIC	homozygous	54208395
7	91835787	91835788	C	T	10	GENIC	homozygous	54021794
7	91836483	91836484	T	A	14	GENIC	homozygous	54021797
7	91837635	91837636	T	C	9	GENIC	homozygous	54021798
7	91837698	91837699	A	G	10	GENIC	homozygous	54021799
7	91840909	91840910	T	C	7	GENIC	homozygous	54021814
7	91841170	91841171	T	C	12	GENIC	homozygous	54021815
7	91842848	91842849	G	T	7	GENIC	homozygous	54208397
7	91843617	91843618	T	C	14	GENIC	possibly homozygous	54021827
7	91844632	91844633	T	G	5	GENIC	heterozygous	54021832
7	91845031	91845032	T	C	6	GENIC	homozygous	54208398
7	91847561	91847562	A	G	12	GENIC	possibly homozygous	54208399
7	91849080	91849081	T	C	2	GENIC	homozygous	54208401
7	91850257	91850258	C	A	2	GENIC	homozygous	54208402
7	91850572	91850573	G	T	17	GENIC	homozygous	54208403