chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31647989	31647990	T	C	43	GENIC	homozygous	116547180
10	31650451	31650452	G	T	33	GENIC	homozygous	116547182
10	31651684	31651685	T	G	40	GENIC	homozygous	116547184
10	31651994	31651995	T	G	53	GENIC	possibly homozygous	116547186
10	31651997	31651998	T	G	56	GENIC	possibly homozygous	116547188
10	31653509	31653510	T	C	55	GENIC	homozygous	116547192
10	31654788	31654789	T	A	45	GENIC	homozygous	116547194
10	31657153	31657154	T	A	45	GENIC	possibly homozygous	116547196
10	31658003	31658004	T	C	45	GENIC	homozygous	117409178
10	31658263	31658264	C	G	34	GENIC	homozygous	117002194
10	31658774	31658775	A	G	44	GENIC	homozygous	116547198
10	31658776	31658777	G	A	44	GENIC	possibly homozygous	116547200
10	31658905	31658906	T	C	66	GENIC	homozygous	116547202
10	31659038	31659039	T	A	49	GENIC	homozygous	116547204
10	31659389	31659390	C	T	60	GENIC	possibly homozygous	116547206
10	31659433	31659434	T	G	59	GENIC	possibly homozygous	116547208