chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	66454808	66454809	C	G	29	GENIC	homozygous	117369166
9	66455828	66455829	A	C	24	GENIC	heterozygous	117783346
9	66457078	66457079	G	A	42	GENIC	homozygous	117369180
9	66457714	66457715	C	T	15	GENIC	homozygous	117369182
9	66459179	66459180	C	T	16	GENIC	homozygous	117369184
9	66460196	66460197	A	G	26	GENIC	homozygous	117369186
9	66460769	66460770	C	A	33	GENIC	homozygous	117369188
9	66461296	66461297	G	A	27	GENIC	homozygous	117369190
9	66464013	66464014	C	T	17	GENIC	homozygous	117369200
9	66464668	66464669	G	A	34	GENIC	homozygous	117369202
9	66467012	66467013	T	C	35	GENIC	homozygous	117369204
9	66467411	66467412	G	A	30	GENIC	homozygous	117369206
9	66467741	66467742	T	C	23	GENIC	homozygous	117369208
9	66469425	66469426	G	C	21	GENIC	homozygous	117369210
9	66469456	66469457	G	A	13	GENIC	homozygous	117369212
9	66470006	66470007	A	C	24	GENIC	homozygous	117369214
9	66471576	66471577	A	G	22	GENIC	homozygous	117369216
9	66472597	66472598	G	C	29	GENIC	homozygous	117369218
9	66472778	66472779	T	G	31	GENIC	homozygous	117369220
9	66475106	66475107	T	A	34	GENIC	homozygous	117369222
9	66476426	66476427	T	A	21	GENIC	possibly homozygous	117369224
9	66477834	66477835	C	T	26	GENIC	homozygous	117369228
9	66479220	66479221	T	G	30	GENIC	homozygous	117369230
9	66480217	66480218	A	G	37	GENIC	homozygous	117369231
9	66480298	66480299	G	A	39	GENIC	homozygous	117369233
9	66480410	66480411	T	G	25	GENIC	homozygous	117369235
9	66481024	66481025	G	T	38	GENIC	homozygous	117369237
9	66482865	66482866	C	T	19	GENIC	homozygous	117369241