chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	265888984	265888985	G	A	48	GENIC	homozygous	109027985
1	265889219	265889219		C	50	GENIC	homozygous	127508966
1	265889539	265889540	A		46	GENIC	possibly homozygous	127508967
1	265889955	265889956	C	G	51	GENIC	homozygous	108637436
1	265890363	265890364	A		47	GENIC	homozygous	127508969
1	265891092	265891092		CCAC	45	GENIC	homozygous	127508970
1	265891407	265891408	G	T	53	GENIC	homozygous	108637438
1	265892140	265892141	G	A	57	GENIC	homozygous	109027987
1	265893145	265893146	A	G	43	GENIC	homozygous	109027988
1	265893438	265893439	C	A	46	GENIC	possibly homozygous	109027989
1	265894447	265894448	G	A	54	GENIC	homozygous	109027990
1	265895083	265895084	C	T	50	GENIC	homozygous	109027991
1	265895666	265895667	G	A	60	GENIC	homozygous	109027992
1	265895735	265895736	A	G	59	GENIC	homozygous	109027993
1	265896026	265896027	A	T	59	GENIC	homozygous	109027994
1	265896028	265896029	C	T	59	GENIC	homozygous	109027995
1	265896135	265896136	C	T	55	GENIC	homozygous	109027996
1	265896986	265896987	T	C	52	GENIC	possibly homozygous	109027997
1	265897137	265897138	T	C	47	GENIC	homozygous	109027998
1	265898993	265898994	C	T	49	GENIC	homozygous	109027999
1	265899444	265899445	T	C	57	GENIC	homozygous	109028000
1	265899477	265899478	A	C	52	GENIC	homozygous	109028001
1	265889796	265889804	ATGTATCC		34	GENIC	homozygous	131267857