chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	157164737	157164738	A	G	55	GENIC	homozygous	114069199
5	157165903	157165904	G	T	42	GENIC	homozygous	114069200
5	157165926	157165927	G	A	42	GENIC	homozygous	114069201
5	157167999	157168000	T	C	44	GENIC	homozygous	114069202
5	157168625	157168626	G	A	64	GENIC	homozygous	114069203
5	157168743	157168744	A	C	57	GENIC	homozygous	114069204
5	157168821	157168822	A	G	63	GENIC	homozygous	114069205
5	157169507	157169508	G	A	52	GENIC	homozygous	114069206
5	157170328	157170329	C	T	57	GENIC	homozygous	114069207
5	157171391	157171392	G	A	45	GENIC	homozygous	114069208
5	157171487	157171488	G	A	43	GENIC	possibly homozygous	114069209
5	157173221	157173222	T	C	44	GENIC	homozygous	114069210
5	157173437	157173438	A	G	47	GENIC	homozygous	114069211
5	157175451	157175452	G	A	43	GENIC	homozygous	114069212
5	157176611	157176612	G	A	56	GENIC	homozygous	114069213
5	157177470	157177471	A	G	62	GENIC	homozygous	114069214
5	157179040	157179041	G	A	59	GENIC	homozygous	114069215
5	157181617	157181618	G	A	41	GENIC	possibly homozygous	114069216
5	157182451	157182452	G	A	19	GENIC	heterozygous	114069217
5	157182706	157182707	G	A	19	GENIC	heterozygous	114069218
5	157183146	157183147	T	A	68	GENIC	homozygous	114069219
5	157186661	157186662	G	A	41	GENIC	homozygous	114069220
5	157187210	157187211	G	A	53	GENIC	homozygous	114069221
5	157187320	157187321	C	A	35	GENIC	homozygous	114069222
5	157187443	157187444	A	G	13	GENIC	homozygous	114069223