chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	46659531	46659532	G	A	29	GENIC	homozygous	117539361
9	46659532	46659533	T	G	29	GENIC	homozygous	117539363
9	46659550	46659550		A	28	GENIC	homozygous	128708313
9	46659570	46659570		A	29	GENIC	homozygous	128708314
9	46659577	46659578	A		30	GENIC	homozygous	128708315
9	46659630	46659631	T		31	GENIC	homozygous	128708316
9	46659639	46659639		T	30	GENIC	homozygous	128708317
9	46659696	46659697	G		33	GENIC	homozygous	128708318
9	46659729	46659730	G	C	31	GENIC	homozygous	117539365
9	46659732	46659733	A		31	GENIC	homozygous	128708319
9	46659752	46659752		T	27	GENIC	homozygous	128708320
9	46659781	46659781		T	28	GENIC	homozygous	128708321
9	46659807	46659808	A		26	GENIC	homozygous	128708322
9	46659856	46659856		C	18	GENIC	homozygous	128708323
9	46659865	46659865		T	17	GENIC	homozygous	128708324
9	46659871	46659871		G	17	GENIC	homozygous	128708325
9	46659892	46659893	G		13	GENIC	homozygous	128708326
9	46659915	46659915		G	8	GENIC	homozygous	128708327
9	46659919	46659920	A	C	7	GENIC	homozygous	117539367
9	46661375	46661376	T	C	27	GENIC	homozygous	117539369
9	46720359	46720359		AGTAAAGTCAAAACTGGATGGTGAGCTTAAAGCCCCCGTCAATCAACCATTG	19	GENIC	homozygous	128708331
9	46728749	46728750	G	T	20	GENIC	homozygous	117539373
9	46728768	46728769	A	T	22	GENIC	homozygous	117333954
9	46728772	46728772		T	21	GENIC	homozygous	128708333
9	46743450	46743450		GTTGTTA	16	GENIC	homozygous	128708334
9	46744607	46744608	G	C	32	GENIC	heterozygous	117333957
9	46744613	46744614	T	G	32	GENIC	heterozygous	117333958
9	46703617	46703618	G	A	34	GENIC	homozygous	120362812
9	46728775	46728776	A	G	21	GENIC	homozygous	117706903
9	46728776	46728777	G	C	21	GENIC	homozygous	117706905
9	46744620	46744621	G	C	35	GENIC	heterozygous	117724807