chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120387249	120387250	G	A	13	GENIC	homozygous	54084081
7	120387941	120387942	T	C	14	GENIC	homozygous	54084082
7	120388694	120388695	A	G	20	GENIC	heterozygous	54084083
7	120389509	120389510	C	T	15	GENIC	homozygous	54084084
7	120389607	120389608	A	G	11	GENIC	homozygous	54084085
7	120389713	120389714	A	G	21	GENIC	homozygous	54084086
7	120390296	120390297	A	G	17	GENIC	homozygous	54084087
7	120390335	120390336	G	A	20	GENIC	heterozygous	54084088
7	120390388	120390389	G	C	18	GENIC	homozygous	54084089
7	120390852	120390853	C	T	15	GENIC	heterozygous	54084090
7	120390927	120390928	T	C	16	GENIC	homozygous	54084091
7	120391170	120391171	A	G	10	GENIC	homozygous	54084092
7	120391780	120391781	A	G	20	GENIC	homozygous	54084093
7	120392222	120392223	G	A	17	GENIC	homozygous	54084094
7	120392714	120392715	C	T	19	GENIC	heterozygous	54084095
7	120392936	120392937	G	A	22	GENIC	heterozygous	54234171
7	120393749	120393750	T	C	15	GENIC	homozygous	54084096
7	120394797	120394798	T	C	7	GENIC	homozygous	54084098
7	120394923	120394924	T	C	13	GENIC	homozygous	54084099
7	120394944	120394945	T	G	8	GENIC	homozygous	54084100
7	120395441	120395442	T	C	13	GENIC	homozygous	54084101