chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	51227911	51227912	G	T	22	GENIC	homozygous	46759707
18	51227989	51227990	C	CTTG	13	GENIC	homozygous	46449709
18	51228306	51228307	T	C	14	GENIC	homozygous	46759708
18	51229836	51229837	T	C	22	GENIC	homozygous	46759709
18	51229985	51229986	T	C	15	GENIC	homozygous	46759710
18	51230181	51230182	G	A	25	GENIC	homozygous	46449712
18	51230988	51230989	C	T	15	GENIC	homozygous	46759711
18	51233337	51233338	G	C	20	GENIC	homozygous	46449715
18	51234599	51234600	G	A	13	GENIC	homozygous	46759712
18	51235044	51235045	A	G	13	GENIC	homozygous	46449716
18	51235163	51235164	T	C	14	GENIC	homozygous	46759713
18	51236667	51236668	C	A	12	GENIC	homozygous	46449717