chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	91588590	91588591	G	A	22	GENIC	possibly homozygous	54021304
7	91588790	91588791	C	T	20	GENIC	possibly homozygous	54021307
7	91588857	91588858	T	-	1	GENIC	homozygous	54021308
7	91589338	91589339	T	C	35	GENIC	possibly homozygous	54661419
7	91590865	91590866	C	A	14	GENIC	homozygous	54021312
7	91591105	91591106	A	G	19	GENIC	homozygous	54021313
7	91591413	91591414	G	C	31	GENIC	possibly homozygous	54661421
7	91591607	91591608	T	C	22	GENIC	homozygous	54021314
7	91591901	91591902	T	C	34	GENIC	possibly homozygous	54021315
7	91591925	91591926	C	-	32	GENIC	possibly homozygous	54208188
7	91591926	91591927	G	T	32	GENIC	possibly homozygous	55143733
7	91592202	91592203	T	C	28	GENIC	homozygous	54208189
7	91592768	91592769	T	A	13	GENIC	homozygous	54021319