chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	9516601	9516602	T	C	26	GENIC	homozygous	112490272
4	9516669	9516670	C	T	29	GENIC	homozygous	112490274
4	9516862	9516863	T	C	24	GENIC	homozygous	112490276
4	9516951	9516952	T	C	34	GENIC	homozygous	112490277
4	9516984	9516985	G	A	38	GENIC	possibly homozygous	112490279
4	9517044	9517045	T	C	56	GENIC	homozygous	112490281
4	9517134	9517135	T	C	54	GENIC	heterozygous	112490283
4	9517167	9517168	A	G	70	GENIC	heterozygous	112490285
4	9517171	9517172	G	A	69	GENIC	heterozygous	112490287
4	9517184	9517185	C	A	70	GENIC	heterozygous	112490289
4	9517294	9517295	A	C	41	GENIC	possibly homozygous	112490293
4	9517186	9517187	C	G	73	GENIC	heterozygous	112996756