chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	264095442	264095443	A	G	26	GENIC	homozygous	108783032
1	264095886	264095887	A	G	31	GENIC	homozygous	108783033
1	264097432	264097433	T	C	47	GENIC	homozygous	108783034
1	264097633	264097634	A	C	29	GENIC	homozygous	108635089
1	264097682	264097683	G	A	30	GENIC	homozygous	108783035
1	264099882	264099883	C	T	31	GENIC	homozygous	108783039
1	264099931	264099932	C	T	24	GENIC	homozygous	108783040
1	264100059	264100060	T	A	34	GENIC	homozygous	108783041
1	264100188	264100189	A	G	30	GENIC	homozygous	108783042
1	264100432	264100433	G	A	40	GENIC	homozygous	108635095
1	264100637	264100638	T	C	27	GENIC	homozygous	108783043
1	264100851	264100852	A	G	35	GENIC	homozygous	120494290
1	264100853	264100854	A	T	34	GENIC	homozygous	120494291
1	264101191	264101192	T	C	17	GENIC	homozygous	108783044
1	264101219	264101220	C	T	10	GENIC	homozygous	108783045
1	264101725	264101726	T	A	25	GENIC	possibly homozygous	108783046
1	264101841	264101842	A	G	19	GENIC	homozygous	108783047
1	264102013	264102014	G	A	28	GENIC	homozygous	108783048
1	264102022	264102023	C	T	27	GENIC	homozygous	108783049
1	264102091	264102092	G	A	39	GENIC	homozygous	108783050
1	264102112	264102113	T	C	41	GENIC	homozygous	108783051
1	264102373	264102374	G	A	26	GENIC	homozygous	108783052
1	264102418	264102419	T	C	26	GENIC	homozygous	108783053
1	264102632	264102633	C	T	28	GENIC	homozygous	108783054
1	264102715	264102716	T	G	23	GENIC	homozygous	109545537
1	264103104	264103105	G	A	36	GENIC	homozygous	108783055
1	264103285	264103286	A	G	17	GENIC	homozygous	108783056
1	264103682	264103683	C	T	31	GENIC	homozygous	108783057
1	264104414	264104415	G	A	38	GENIC	homozygous	108783058
1	264105443	264105444	A	C	36	GENIC	homozygous	108783059