chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	264094261	264094262	T	C	28	GENIC	possibly homozygous	109217854
1	264095002	264095003	T	C	31	GENIC	possibly homozygous	109217858
1	264095472	264095473	T	C	33	GENIC	homozygous	120905090
1	264096218	264096219	C	T	36	GENIC	possibly homozygous	120905091
1	264096731	264096732	G	A	32	GENIC	homozygous	120905092
1	264097115	264097116	C	T	24	GENIC	homozygous	120905093
1	264097200	264097201	G	A	35	GENIC	possibly homozygous	120905094
1	264097208	264097209	T	C	35	GENIC	possibly homozygous	120905095
1	264097633	264097634	A	C	39	GENIC	homozygous	108635089
1	264097432	264097433	T	C	19	GENIC	homozygous	108783034
1	264095886	264095887	A	G	29	GENIC	possibly homozygous	108783033
1	264098036	264098037	G	T	26	GENIC	possibly homozygous	120905096
1	264098042	264098043	G	A	25	GENIC	possibly homozygous	120905097
1	264098403	264098404	T	C	20	GENIC	homozygous	120905098
1	264098424	264098425	G	A	23	GENIC	homozygous	120905099
1	264099176	264099177	G	A	18	GENIC	possibly homozygous	120905100
1	264099576	264099577	C	T	11	GENIC	possibly homozygous	120905101
1	264099875	264099876	C	T	35	GENIC	possibly homozygous	120905102
1	264100059	264100060	T	A	27	GENIC	homozygous	108783041
1	264100188	264100189	A	G	23	GENIC	homozygous	108783042
1	264100212	264100213	T	G	20	GENIC	possibly homozygous	108635093
1	264100452	264100453	C	A	25	GENIC	possibly homozygous	120905103
1	264100637	264100638	T	C	36	GENIC	homozygous	108783043
1	264100695	264100696	G	A	35	GENIC	possibly homozygous	120905104
1	264101486	264101487	C	G	5	GENIC	homozygous	120905105
1	264103421	264103422	C	T	30	GENIC	homozygous	120905106
1	264105400	264105401	T	G	35	GENIC	possibly homozygous	120905107
1	264105443	264105444	A	C	26	GENIC	homozygous	108783059