chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	265290448	265290449	G	A	16	GENIC	homozygous	108636938
1	265290481	265290482	C	T	24	GENIC	homozygous	109027780
1	265290684	265290685	A	G	39	GENIC	homozygous	108636939
1	265290865	265290866	T	C	24	GENIC	homozygous	108636940
1	265291237	265291238	T	C	24	GENIC	homozygous	108636941
1	265291484	265291485	T	C	36	GENIC	homozygous	108636942
1	265291873	265291874	T	A	27	GENIC	homozygous	108636943
1	265292034	265292035	G	A	22	GENIC	homozygous	109027781
1	265292526	265292527	G	A	29	GENIC	homozygous	109027782
1	265293507	265293508	C	T	49	GENIC	homozygous	108636944
1	265295018	265295019	C	T	18	GENIC	possibly homozygous	109027783
1	265295051	265295052	G	T	13	GENIC	heterozygous	109027784
1	265295066	265295067	C	T	21	GENIC	possibly homozygous	109027785
1	265295133	265295134	G	T	19	GENIC	homozygous	108636946
1	265296127	265296128	A	G	32	GENIC	homozygous	108636947
1	265297262	265297263	T	C	13	GENIC	possibly homozygous	108636948
1	265298482	265298483	C	T	29	GENIC	homozygous	109027786
1	265298829	265298830	G	A	17	GENIC	homozygous	109058207
1	265295028	265295029	A	G	11	GENIC	heterozygous	109058205
1	265295035	265295036	G	T	15	GENIC	heterozygous	109058206