chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263449011	263449012	G	T	21	GENIC	homozygous	109027024
1	263449595	263449596	T	A	16	GENIC	homozygous	109027025
1	263450387	263450388	A	G	18	GENIC	homozygous	108633075
1	263451228	263451231	TGC		10	GENIC	homozygous	131267624
1	263451566	263451567	A	G	19	GENIC	homozygous	109027026
1	263451751	263451754	AAG		8	GENIC	homozygous	132543174
1	263452091	263452098	GCCATGG		15	GENIC	homozygous	132543175
1	263452150	263452151	T	G	16	GENIC	homozygous	109027027
1	263452284	263452284		A	21	GENIC	homozygous	131267625
1	263452587	263452587		TTTTAAACAACC	8	GENIC	homozygous	131267626
1	263453135	263453136	A	G	8	GENIC	homozygous	108633083
1	263454812	263454813	G	A	21	GENIC	homozygous	109027029
1	263455081	263455082	G	A	11	GENIC	homozygous	109027030
1	263455588	263455589	A	T	19	GENIC	homozygous	108633087
1	263455726	263455727	A	G	23	GENIC	homozygous	109027031
1	263457421	263457422	C	A	19	GENIC	homozygous	109027038
1	263457693	263457694	G	A	22	GENIC	homozygous	109027039
1	263458131	263458132	T	G	22	GENIC	homozygous	108633093
1	263459229	263459230	G	A	21	GENIC	homozygous	108633095
1	263459232	263459232		A	21	GENIC	homozygous	127508012
1	263459234	263459235	G	C	22	GENIC	homozygous	108633097