chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	266078160	266078161	A	G	21	GENIC	homozygous	108637501
1	266078759	266078760	A	G	27	GENIC	homozygous	108637502
1	266079369	266079370	C	T	28	GENIC	homozygous	108637503
1	266080594	266080595	C	T	16	GENIC	homozygous	108637504
1	266080836	266080837	G	T	28	GENIC	homozygous	108637505
1	266081684	266081685	T	C	28	GENIC	homozygous	108637506
1	266081837	266081838	G	A	31	GENIC	homozygous	108637507
1	266081910	266081911	T	C	37	GENIC	homozygous	108637508
1	266081962	266081963	C	T	34	GENIC	homozygous	108637509
1	266082097	266082098	A	G	50	GENIC	homozygous	108637510
1	266082594	266082595	G	T	12	GENIC	homozygous	108637511
1	266082719	266082720	A	G	28	GENIC	homozygous	108637512
1	266082922	266082923	C	T	27	GENIC	homozygous	108637513
1	266083400	266083401	T	C	30	GENIC	homozygous	108637514
1	266084034	266084035	A	G	32	GENIC	homozygous	108637516
1	266084358	266084359	G	A	23	GENIC	homozygous	108637517
1	266085294	266085295	A	G	20	GENIC	possibly homozygous	108637518