chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120387249	120387250	G	A	15	GENIC	homozygous	54084081
7	120387941	120387942	T	C	14	GENIC	possibly homozygous	54084082
7	120389509	120389510	C	T	10	GENIC	heterozygous	54084084
7	120389607	120389608	A	G	14	GENIC	homozygous	54084085
7	120389713	120389714	A	G	26	GENIC	possibly homozygous	54084086
7	120390296	120390297	A	G	24	GENIC	homozygous	54084087
7	120390388	120390389	G	C	14	GENIC	homozygous	54084089
7	120390927	120390928	T	C	18	GENIC	possibly homozygous	54084091
7	120391170	120391171	A	G	14	GENIC	possibly homozygous	54084092
7	120391780	120391781	A	G	20	GENIC	homozygous	54084093
7	120392222	120392223	G	A	31	GENIC	possibly homozygous	54084094
7	120392936	120392937	G	A	16	GENIC	possibly homozygous	54234171
7	120393749	120393750	T	C	18	GENIC	possibly homozygous	54084096
7	120394797	120394798	T	C	8	GENIC	possibly homozygous	54084098
7	120394923	120394924	T	C	10	GENIC	homozygous	54084099
7	120394944	120394945	T	G	7	GENIC	homozygous	54084100
7	120395441	120395442	T	C	14	GENIC	homozygous	54084101
7	120396585	120396586	T	TC	3	GENIC	heterozygous	54234175