chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	51225788	51225789	A	G	15	GENIC	homozygous	46449693
18	51226096	51226097	T	C	23	GENIC	homozygous	46759706
18	51227911	51227912	G	T	9	GENIC	homozygous	46759707
18	51227989	51227990	C	CTTG	10	GENIC	homozygous	46449709
18	51228306	51228307	T	C	12	GENIC	homozygous	46759708
18	51229836	51229837	T	C	16	GENIC	homozygous	46759709
18	51229873	51229874	C	CTTTATTTATTTA	7	GENIC	homozygous	46449711
18	51229985	51229986	T	C	17	GENIC	homozygous	46759710
18	51230181	51230182	G	A	14	GENIC	homozygous	46449712
18	51230988	51230989	C	T	6	GENIC	homozygous	46759711
18	51233337	51233338	G	C	14	GENIC	homozygous	46449715
18	51234599	51234600	G	A	15	GENIC	homozygous	46759712
18	51235044	51235045	A	G	19	GENIC	homozygous	46449716
18	51235163	51235164	T	C	16	GENIC	homozygous	46759713
18	51236667	51236668	C	A	19	GENIC	homozygous	46449717
18	51237768	51237769	T	A	19	GENIC	homozygous	46449718
18	51237841	51237842	T	TATTC	12	GENIC	homozygous	46449721
18	51238400	51238401	T	C	19	GENIC	possibly homozygous	46449722
18	51239800	51239801	G	GA	16	GENIC	homozygous	46449723
18	51240150	51240152	TT	--	10	GENIC	heterozygous	46687690
18	51240151	51240152	T	-	10	GENIC	heterozygous	46759714
18	51240961	51240962	A	G	14	GENIC	homozygous	46449725
18	51241908	51241909	A	G	16	GENIC	possibly homozygous	46449727
18	51242025	51242026	G	A	22	GENIC	homozygous	46759715
18	51242209	51242210	A	G	13	GENIC	homozygous	46759716
18	51242388	51242389	C	T	19	GENIC	homozygous	46759717
18	51242608	51242609	A	C	22	GENIC	homozygous	46759718
18	51243135	51243136	T	C	18	GENIC	homozygous	46759719
18	51243389	51243390	G	T	32	GENIC	homozygous	46759720