chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130117240	130117241	C	A	57	GENIC	possibly homozygous	54110353
7	130118246	130118247	T	-	66	GENIC	homozygous	54110354
7	130118274	130118275	C	A	69	GENIC	homozygous	54110355
7	130120300	130120301	A	G	64	GENIC	homozygous	54110356
7	130120410	130120411	C	CTTT	29	GENIC	heterozygous	54110357
7	130120410	130120411	C	CTT	29	GENIC	heterozygous	54110358
7	130120484	130120485	G	C	38	GENIC	homozygous	54110359
7	130120642	130120643	T	C	63	GENIC	homozygous	54110360
7	130121330	130121331	A	G	39	GENIC	homozygous	54110361
7	130121351	130121352	C	CAGGCCTGATTCAG	28	GENIC	homozygous	54110362
7	130121574	130121575	C	T	51	GENIC	homozygous	54110363
7	130121716	130121717	A	G	51	GENIC	homozygous	54110364
7	130121749	130121750	A	G	43	GENIC	homozygous	54110365
7	130124264	130124265	T	C	51	GENIC	homozygous	54110366
7	130124636	130124637	G	A	61	GENIC	homozygous	54110367