chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117052890	117052891	A	G	9	GENIC	heterozygous	52829228
8	117054122	117054123	C	T	14	GENIC	heterozygous	52829230
8	117054158	117054159	A	G	10	GENIC	heterozygous	52829231
8	117056327	117056328	C	A	32	GENIC	heterozygous	52829242
8	117056459	117056460	G	A	33	GENIC	heterozygous	52829243
8	117057218	117057219	T	-	25	GENIC	heterozygous	52829244
8	117058388	117058389	A	G	23	GENIC	heterozygous	52829245
8	117059204	117059205	A	C	35	GENIC	heterozygous	52829246
8	117060807	117060808	C	T	20	GENIC	heterozygous	52829248
8	117061256	117061257	C	T	19	GENIC	heterozygous	52829250
8	117061986	117061987	C	T	6	GENIC	heterozygous	52829251
8	117062340	117062341	T	TGTCA	31	GENIC	heterozygous	52829253
8	117062839	117062840	C	G	47	GENIC	heterozygous	52829254
8	117067190	117067191	G	GCTGT	28	GENIC	heterozygous	52829260
8	117067250	117067251	A	G	16	GENIC	heterozygous	52829261
8	117067587	117067588	T	C	20	GENIC	heterozygous	52829262
8	117068510	117068511	A	G	23	GENIC	heterozygous	52829263
8	117068680	117068681	C	A	29	GENIC	heterozygous	52829265
8	117068800	117068801	A	G	16	GENIC	heterozygous	52829266
8	117068936	117068937	T	TTC	9	GENIC	heterozygous	52829267
8	117074996	117074997	A	G	23	GENIC	heterozygous	52829280