chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	95935898	95935899	C	T	67	GENIC	homozygous	66165069
13	95937472	95937473	T	G	33	GENIC	heterozygous	66165072
13	95938200	95938201	T	C	26	GENIC	homozygous	66165075
13	95938755	95938756	G	A	67	GENIC	possibly homozygous	66165078
13	95939435	95939436	T	C	57	GENIC	homozygous	66165081
13	95940242	95940243	A	G	30	GENIC	homozygous	66165084
13	95940761	95940762	C	T	51	GENIC	possibly homozygous	66165087
13	95940958	95940959	C	T	6	GENIC	homozygous	66165090
13	95941060	95941061	A	G	20	GENIC	homozygous	66165093
13	95942441	95942442	C	T	6	GENIC	homozygous	66165096
13	95942541	95942542	A	G	47	GENIC	homozygous	66165099
13	95943575	95943576	T	C	65	GENIC	homozygous	66165102
13	95943955	95943956	C	T	49	GENIC	homozygous	66165105
13	95944184	95944185	T	C	25	GENIC	homozygous	66165108
13	95944375	95944376	A	G	60	GENIC	homozygous	66165111
13	95945760	95945761	A	G	37	GENIC	homozygous	66165114
13	95948443	95948444	T	C	56	GENIC	homozygous	66165117
13	95948856	95948857	T	C	41	GENIC	heterozygous	66165120
13	95948927	95948928	G	A	23	GENIC	heterozygous	66165123
13	95948935	95948936	G	A	20	GENIC	heterozygous	66165126
13	95948939	95948940	G	A	18	GENIC	heterozygous	66165129
13	95949433	95949434	G	T	27	GENIC	homozygous	66165132
13	95950781	95950782	T	C	39	GENIC	homozygous	66165135
13	95950851	95950852	G	C	58	GENIC	homozygous	66165138