chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	71900936	71900937	C	T	13	GENIC	homozygous	63932759
18	71900969	71900970	C	T	13	GENIC	homozygous	63932760
18	71901284	71901285	C	G	4	GENIC	homozygous	63932761
18	71901305	71901306	C	G	9	GENIC	homozygous	84622212
18	71901306	71901307	G	C	9	GENIC	homozygous	84622213
18	71901313	71901314	A	G	10	GENIC	possibly homozygous	63932764
18	71901314	71901315	C	A	10	GENIC	possibly homozygous	64232095
18	71901448	71901449	G	T	19	GENIC	homozygous	63932766
18	71951361	71951362	G	A	19	GENIC	heterozygous	63932779
18	71953459	71953460	C	T	7	GENIC	heterozygous	63932781
18	72036909	72036910	C	A	10	GENIC	heterozygous	64612242