chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120393276	120393277	G	A	31	GENIC	homozygous	54859820
7	120393749	120393750	T	C	29	GENIC	homozygous	54084096
7	120394682	120394683	A	ACAGCTAGAC	23	GENIC	homozygous	54084097
7	120394797	120394798	T	C	27	GENIC	homozygous	54084098
7	120394923	120394924	T	C	12	GENIC	homozygous	54084099
7	120394944	120394945	T	G	10	GENIC	homozygous	54084100
7	120395441	120395442	T	C	33	GENIC	homozygous	54084101
7	120395946	120395947	T	TG	16	GENIC	possibly homozygous	54084102
7	120395961	120395962	T	TTTG	16	GENIC	heterozygous	54084103
7	120398835	120398836	C	CGTGTGTGT	16	INTERGENIC	homozygous	54084105
7	120398935	120398936	C	T	31	INTERGENIC	homozygous	54859821
7	120399434	120399435	G	A	14	INTERGENIC	homozygous	54084106
7	120399450	120399451	A	G	15	INTERGENIC	homozygous	54084107
7	120399540	120399541	G	A	21	INTERGENIC	homozygous	54084108
7	120399996	120399997	T	A	13	INTERGENIC	homozygous	54084110
7	120400039	120400040	T	C	14	INTERGENIC	homozygous	54084111
7	120400336	120400337	C	CTG	35	INTERGENIC	homozygous	54084112
7	120400502	120400503	G	A	25	INTERGENIC	homozygous	54084113
7	120400517	120400518	A	G	27	INTERGENIC	homozygous	54084114
7	120400659	120400660	C	T	21	INTERGENIC	homozygous	54084115
7	120400735	120400736	G	A	25	INTERGENIC	possibly homozygous	54084116
7	120400751	120400752	A	T	25	INTERGENIC	possibly homozygous	54084117
7	120400864	120400865	C	T	15	INTERGENIC	possibly homozygous	54084118
7	120401158	120401159	A	G	35	INTERGENIC	homozygous	54084119
7	120402309	120402310	T	C	41	INTERGENIC	homozygous	54084120
7	120395961	120395962	T	TG	16	GENIC	possibly homozygous	55001602