chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	261495864	261495865	T	A	49	GENIC	homozygous	108629655
1	261498157	261498158	G	A	65	GENIC	homozygous	108629656
1	261499518	261499519	C	T	62	GENIC	homozygous	108629657
1	261499840	261499841	A	G	16	GENIC	possibly homozygous	108629658
1	261500375	261500376	G	A	78	GENIC	homozygous	108629659
1	261501204	261501205	G	C	46	GENIC	homozygous	108629661
1	261501213	261501214	A	C	47	GENIC	possibly homozygous	108629662
1	261501606	261501607	T	A	45	GENIC	possibly homozygous	108629663
1	261501902	261501903	C	T	48	GENIC	homozygous	108629664
1	261502293	261502294	C	T	69	GENIC	homozygous	108629665
1	261502887	261502888	G	T	43	GENIC	homozygous	108629666
1	261503740	261503741	C	T	63	GENIC	homozygous	108629667
1	261504401	261504402	T	C	55	GENIC	possibly homozygous	108629668
1	261504617	261504618	T	C	62	GENIC	homozygous	108629669
1	261504672	261504673	G	A	68	GENIC	homozygous	108629670
1	261504845	261504846	G	A	89	GENIC	possibly homozygous	108629671
1	261505056	261505057	T	G	56	GENIC	homozygous	108629672
1	261505378	261505379	G	A	33	GENIC	heterozygous	108629673
1	261505398	261505399	C	T	34	GENIC	homozygous	108629674
1	261506207	261506208	A	G	56	GENIC	homozygous	108629675
1	261506815	261506816	A	G	81	GENIC	heterozygous	108629676
1	261507255	261507256	G	A	46	GENIC	homozygous	108629677
1	261507668	261507669	A	T	33	GENIC	homozygous	108629678
1	261508302	261508303	G	T	53	GENIC	possibly homozygous	108629679
1	261509654	261509655	G	A	72	GENIC	homozygous	108629680
1	261510735	261510736	C	T	55	GENIC	homozygous	108629681
1	261511563	261511564	G	T	33	GENIC	homozygous	108629682
1	261511970	261511971	C	T	36	GENIC	homozygous	108629683
1	261512010	261512011	C	G	34	GENIC	heterozygous	108629684
1	261512540	261512541	G	A	49	GENIC	homozygous	108629685
1	261514007	261514008	T	C	68	GENIC	homozygous	108629686