chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117458900	117458901	C		14	GENIC	homozygous	128635832
8	117460914	117460915	G	T	20	GENIC	homozygous	116671504
8	117462354	117462355	C	T	22	GENIC	homozygous	116671506
8	117463142	117463143	A	G	28	GENIC	homozygous	116671508
8	117463763	117463764	C	T	17	GENIC	homozygous	116671510
8	117464601	117464602	T	C	24	GENIC	homozygous	116671516
8	117464876	117464877	G	A	23	GENIC	homozygous	116671518
8	117466249	117466250	A	C	24	GENIC	homozygous	116671520
8	117466513	117466514	T	C	16	GENIC	homozygous	116671522
8	117466898	117466898		GG	6	GENIC	homozygous	128635833
8	117467952	117467953	A	G	7	GENIC	homozygous	116671528
8	117468441	117468442	G	A	19	GENIC	homozygous	116671530
8	117468564	117468565	G	A	17	GENIC	homozygous	116671532
8	117468864	117468865	C	G	3	GENIC	homozygous	116671534
8	117469362	117469363	T	C	18	GENIC	homozygous	116671536
8	117470014	117470015	T	C	16	GENIC	homozygous	116671538
8	117470387	117470388	G	A	12	GENIC	homozygous	116671540
8	117471283	117471284	T	C	32	GENIC	homozygous	116671542
8	117471357	117471358	A	T	29	GENIC	homozygous	116671544
8	117471931	117471932	T	G	14	GENIC	homozygous	116671546
8	117471948	117471949	G	T	14	GENIC	homozygous	116671548
8	117472015	117472016	T	C	10	GENIC	homozygous	116671552
8	117472671	117472672	G		22	GENIC	homozygous	128635834
8	117473215	117473216	G	A	21	GENIC	homozygous	116671554
8	117473754	117473754		CCTCCCCAT	8	GENIC	homozygous	128635835
8	117473789	117473790	A	G	15	GENIC	homozygous	116671556
8	117473918	117473919	A	T	24	GENIC	homozygous	116671568
8	117473986	117473987	C	T	25	GENIC	homozygous	116671574
8	117474113	117474114	C	T	24	GENIC	heterozygous	129956039
8	117475110	117475111	C	A	21	GENIC	homozygous	116671590