chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	119054689	119054690	C	CGTGT	14	INTERGENIC	possibly homozygous	54232158
7	119055128	119055129	G	GTTC	25	INTERGENIC	homozygous	54080364
7	119055234	119055235	G	GA	22	INTERGENIC	homozygous	54750682
7	119056013	119056014	A	C	28	INTERGENIC	homozygous	54080365
7	119056280	119056281	A	G	25	INTERGENIC	homozygous	54080366
7	119057324	119057325	T	C	18	INTERGENIC	homozygous	54232164
7	119057605	119057606	C	A	39	INTERGENIC	possibly homozygous	54750684
7	119060355	119060356	T	TTTTTG	20	INTERGENIC	homozygous	54750686
7	119060676	119060680	CCCT	----	30	INTERGENIC	homozygous	54080373
7	119061433	119061434	G	GT	11	INTERGENIC	heterozygous	54080375
7	119061434	119061435	G	GT	11	INTERGENIC	heterozygous	54080376
7	119061805	119061806	C	T	33	INTERGENIC	possibly homozygous	54750688
7	119062366	119062367	A	G	31	INTERGENIC	homozygous	54750690
7	119062556	119062557	A	G	26	INTERGENIC	homozygous	54750692
7	119063659	119063660	T	G	22	INTERGENIC	homozygous	54080378
7	119063859	119063860	T	C	26	INTERGENIC	homozygous	54750694
7	119065285	119065286	C	T	37	INTERGENIC	homozygous	54750696
7	119066563	119066564	A	G	18	INTERGENIC	homozygous	54750698
7	119066575	119066576	C	CGG	9	INTERGENIC	heterozygous	54080381
7	119066602	119066603	C	T	18	INTERGENIC	homozygous	54750700
7	119067033	119067034	C	A	36	INTERGENIC	homozygous	54750702
7	119066575	119066576	C	CGGG	9	INTERGENIC	heterozygous	54586959