chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	226622296	226622297	C	T	2	GENIC	homozygous	120595712
1	226622297	226622298	C	T	2	GENIC	homozygous	120595714
1	226622471	226622472	A	G	21	GENIC	possibly homozygous	108558817
1	226625004	226625005	C	G	32	GENIC	homozygous	120595716
1	226626679	226626680	C	T	17	GENIC	homozygous	120595718
1	226626795	226626796	G	A	27	GENIC	possibly homozygous	120595720
1	226627074	226627075	C	A	25	GENIC	homozygous	120876549
1	226627987	226627988	C	G	36	GENIC	homozygous	120595722
1	226629244	226629245	A	G	25	GENIC	possibly homozygous	120595725
1	226631089	226631090	T	A	22	GENIC	possibly homozygous	120876550
1	226631979	226631980	T	C	20	GENIC	homozygous	108558819
1	226632065	226632066	T	C	23	GENIC	homozygous	108558820
1	226632174	226632175	T	G	30	GENIC	possibly homozygous	108558822
1	226632517	226632518	C	T	26	GENIC	possibly homozygous	108558823
1	226632623	226632624	G	A	30	GENIC	possibly homozygous	120876551
1	226632974	226632975	G	A	39	GENIC	possibly homozygous	108558824
1	226634743	226634744	C	A	20	GENIC	homozygous	108558827
1	226635194	226635195	G	A	23	GENIC	possibly homozygous	108558828
1	226635792	226635793	A	G	39	GENIC	homozygous	108558829
1	226637997	226637998	A	C	26	GENIC	homozygous	108558835
1	226638159	226638160	A	G	26	GENIC	homozygous	120876552
1	226638813	226638814	A	T	31	GENIC	possibly homozygous	108558836
1	226638839	226638840	G	C	32	GENIC	possibly homozygous	108558837
1	226639578	226639579	T	C	38	GENIC	possibly homozygous	108558839
1	226639699	226639700	G	T	30	GENIC	possibly homozygous	108558840
1	226640186	226640187	A	G	8	GENIC	homozygous	120902502
1	226640189	226640190	A	G	8	GENIC	homozygous	120902503
1	226640192	226640193	A	G	8	GENIC	homozygous	120595727
1	226640195	226640196	A	G	9	GENIC	homozygous	120595729
1	226640198	226640199	A	G	9	GENIC	homozygous	120490658
1	226640970	226640971	T	C	23	GENIC	homozygous	108558842
1	226641283	226641284	A	G	38	GENIC	possibly homozygous	108558843