chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	79666884	79666885	T		11	GENIC	heterozygous	130572346
9	79673610	79673611	T		2	GENIC	homozygous	128726902
9	79672760	79672760		TGTTC	4	GENIC	homozygous	128726900
9	79673587	79673597	TCCCCGCTCA		1	GENIC	homozygous	128726901
9	79673615	79673615		A	2	GENIC	homozygous	128726903
9	79673629	79673632	GGG		2	GENIC	homozygous	128726904
9	79673636	79673637	G		2	GENIC	homozygous	128726905
9	79673669	79673670	C		3	GENIC	homozygous	128726906
9	79673676	79673678	TA		3	GENIC	homozygous	128726907
9	79673680	79673682	CC		3	GENIC	homozygous	128726908
9	79673691	79673691		C	4	GENIC	homozygous	128726909
9	79673696	79673696		T	4	GENIC	homozygous	128726910
9	79673708	79673708		T	6	GENIC	homozygous	128726911
9	79673716	79673716		C	6	GENIC	homozygous	128726912
9	79727428	79727429	G		8	GENIC	homozygous	128726913
9	79727431	79727432	G		9	GENIC	homozygous	128726914
9	79727497	79727498	A		3	GENIC	homozygous	128726915
9	79727502	79727503	A		3	GENIC	homozygous	128726916
9	79727538	79727539	C		2	GENIC	homozygous	128726917
9	79736688	79736689	C		10	GENIC	homozygous	128726923
9	79736692	79736693	C		10	GENIC	homozygous	128726924
9	79673667	79673668	A	T	3	GENIC	homozygous	117809024
9	79727508	79727509	G	A	3	GENIC	homozygous	117380750
9	79727512	79727513	T	G	3	GENIC	homozygous	117380751
9	79746560	79746561	C	A	7	GENIC	homozygous	128774622