chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117052068	117052069	A	G	14	GENIC	heterozygous	53222549
8	117052890	117052891	A	G	27	GENIC	heterozygous	52829228
8	117054122	117054123	C	T	8	GENIC	heterozygous	52829230
8	117054158	117054159	A	G	12	GENIC	heterozygous	52829231
8	117055685	117055686	C	T	10	GENIC	heterozygous	52829240
8	117058726	117058727	C	T	27	GENIC	heterozygous	53222551
8	117062340	117062341	T	TGTCA	42	GENIC	heterozygous	52829253
8	117065011	117065012	A	G	34	GENIC	heterozygous	53222553
8	117067190	117067191	G	GCTGT	25	GENIC	heterozygous	52829260
8	117067250	117067251	A	G	29	GENIC	heterozygous	52829261
8	117067587	117067588	T	C	25	GENIC	heterozygous	52829262
8	117068680	117068681	C	A	31	GENIC	heterozygous	52829265
8	117068800	117068801	A	G	29	GENIC	heterozygous	52829266
8	117068936	117068937	T	TTC	23	GENIC	heterozygous	52829267
8	117071534	117071535	C	T	15	GENIC	heterozygous	53222559
8	117071896	117071897	G	A	13	GENIC	heterozygous	53222560
8	117072006	117072007	C	T	13	GENIC	heterozygous	53222561
8	117072252	117072253	A	AG	16	GENIC	heterozygous	53222562
8	117072978	117072979	A	G	29	GENIC	heterozygous	53222566
8	117074996	117074997	A	G	29	GENIC	heterozygous	52829280