chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	79672760	79672760		TGTTC	11	GENIC	homozygous	128726900
9	79672927	79672928	A		3	GENIC	homozygous	130773433
9	79673587	79673597	TCCCCGCTCA		1	GENIC	homozygous	128726901
9	79673610	79673611	T		1	GENIC	homozygous	128726902
9	79673615	79673615		A	1	GENIC	homozygous	128726903
9	79673629	79673632	GGG		1	GENIC	homozygous	128726904
9	79673636	79673637	G		1	GENIC	homozygous	128726905
9	79673667	79673668	A	T	3	GENIC	homozygous	117809024
9	79673669	79673670	C		3	GENIC	homozygous	128726906
9	79673676	79673678	TA		3	GENIC	homozygous	128726907
9	79673680	79673682	CC		5	GENIC	homozygous	128726908
9	79673691	79673691		C	6	GENIC	homozygous	128726909
9	79673696	79673696		T	6	GENIC	homozygous	128726910
9	79673708	79673708		T	13	GENIC	homozygous	128726911
9	79673716	79673716		C	13	GENIC	homozygous	128726912
9	79727428	79727429	G		10	GENIC	homozygous	128726913
9	79727431	79727432	G		9	GENIC	homozygous	128726914
9	79727497	79727498	A		5	GENIC	homozygous	128726915
9	79727502	79727503	A		5	GENIC	homozygous	128726916
9	79727508	79727509	G	A	3	GENIC	homozygous	117380750
9	79727512	79727513	T	G	3	GENIC	homozygous	117380751
9	79727538	79727539	C		1	GENIC	homozygous	128726917
9	79727585	79727585		C	3	GENIC	homozygous	128726918
9	79727602	79727603	C		3	GENIC	homozygous	128726919
9	79727616	79727617	G	T	5	GENIC	homozygous	123203952
9	79727617	79727618	T	G	5	GENIC	homozygous	123203953
9	79727632	79727633	A	T	6	GENIC	homozygous	123203954
9	79727633	79727634	T	A	6	GENIC	homozygous	123203955
9	79727665	79727665		A	8	GENIC	homozygous	128726920
9	79727667	79727668	G		8	GENIC	homozygous	128726921
9	79727675	79727676	T	A	8	GENIC	homozygous	123203960
9	79727677	79727678	C		8	GENIC	homozygous	128726922
9	79727690	79727691	G	A	8	GENIC	homozygous	117594054
9	79727691	79727692	A	G	8	GENIC	homozygous	123203962
9	79736688	79736689	C		15	GENIC	homozygous	128726923
9	79736692	79736693	C		15	GENIC	homozygous	128726924
9	79746560	79746561	C	A	11	GENIC	homozygous	128774622