chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	119701430	119701431	A	G	1	GENIC	homozygous	54082051
7	119701440	119701441	G	A	3	GENIC	homozygous	54082052
7	119701543	119701544	C	T	23	GENIC	homozygous	54082053
7	119701611	119701612	A	G	19	GENIC	heterozygous	54082054
7	119701995	119701996	C	T	14	GENIC	homozygous	54082055
7	119702044	119702045	C	-	3	GENIC	homozygous	54082056
7	119702046	119702047	C	T	4	GENIC	homozygous	54920984
7	119702090	119702091	C	G	16	GENIC	possibly homozygous	54082057
7	119702157	119702158	C	T	18	GENIC	homozygous	54082058
7	119702344	119702345	T	C	15	GENIC	homozygous	54082059
7	119702691	119702692	G	GGAGCCCGGAAGGCAACT	7	GENIC	possibly homozygous	54082060
7	119702748	119702749	T	C	28	GENIC	homozygous	54082062
7	119703416	119703417	A	G	10	GENIC	homozygous	54082063
7	119705272	119705273	T	C	27	GENIC	possibly homozygous	54082064
7	119706360	119706361	A	G	25	INTERGENIC	homozygous	54082065
7	119706498	119706499	G	GACACACAC	11	INTERGENIC	homozygous	54920986
7	119706543	119706544	A	C	14	INTERGENIC	possibly homozygous	54082067
7	119707003	119707004	T	C	22	INTERGENIC	possibly homozygous	54082068
7	119708675	119708676	G	A	17	INTERGENIC	possibly homozygous	54082071
7	119713692	119713693	C	T	25	INTERGENIC	homozygous	54082074
7	119714298	119714299	A	G	15	INTERGENIC	homozygous	54082075
7	119715751	119715752	C	T	19	INTERGENIC	homozygous	54082077
7	119716047	119716048	A	G	19	INTERGENIC	possibly homozygous	54082078