chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	95935898	95935899	C	T	30	GENIC	homozygous	66165069
13	95938200	95938201	T	C	21	GENIC	homozygous	66165075
13	95938755	95938756	G	A	15	GENIC	homozygous	66165078
13	95939435	95939436	T	C	19	GENIC	homozygous	66165081
13	95940242	95940243	A	G	19	GENIC	homozygous	66165084
13	95940761	95940762	C	T	5	GENIC	homozygous	66165087
13	95941060	95941061	A	G	11	GENIC	homozygous	66165093
13	95942541	95942542	A	G	18	GENIC	homozygous	66165099
13	95943575	95943576	T	C	33	GENIC	homozygous	66165102
13	95943955	95943956	C	T	20	GENIC	homozygous	66165105
13	95944184	95944185	T	C	15	GENIC	homozygous	66165108
13	95944375	95944376	A	G	19	GENIC	homozygous	66165111
13	95948443	95948444	T	C	18	GENIC	homozygous	66165117
13	95948856	95948857	T	C	19	GENIC	heterozygous	66165120
13	95948923	95948924	G	A	16	GENIC	homozygous	67643813
13	95948927	95948928	G	A	16	GENIC	homozygous	66165123
13	95950781	95950782	T	C	18	GENIC	homozygous	66165135
13	95950851	95950852	G	C	27	GENIC	homozygous	66165138
13	95948919	95948920	G	A	16	GENIC	homozygous	66590318