chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	226530363	226530364	C	T	18	GENIC	homozygous	59420829
2	226530704	226530705	A	G	16	GENIC	homozygous	60245514
2	226531011	226531012	G	A	34	GENIC	homozygous	59420833
2	226531529	226531530	G	GT	27	GENIC	homozygous	59420835
2	226531944	226531945	C	G	32	GENIC	homozygous	59420836
2	226533032	226533033	A	C	29	GENIC	homozygous	59420838
2	226533755	226533756	C	T	29	GENIC	homozygous	60245516
2	226534870	226534871	A	T	33	GENIC	homozygous	59420846
2	226538482	226538483	A	G	17	GENIC	possibly homozygous	60245518
2	226538539	226538540	C	-	21	GENIC	homozygous	59420859
2	226538659	226538660	C	T	20	GENIC	possibly homozygous	60245520
2	226539569	226539570	C	G	30	GENIC	homozygous	60245522
2	226540380	226540381	G	C	21	GENIC	homozygous	59420870
2	226540439	226540440	G	A	29	GENIC	homozygous	59420872
2	226541513	226541514	T	-	25	GENIC	homozygous	59420876
2	226541701	226541702	C	A	34	GENIC	homozygous	59420878
2	226541817	226541818	C	T	27	GENIC	possibly homozygous	60245524
2	226542180	226542181	A	-	24	GENIC	possibly homozygous	60245526
2	226542792	226542793	T	TA	34	GENIC	homozygous	60245528
2	226542793	226542794	T	TA	34	GENIC	homozygous	60245530
2	226542891	226542892	C	T	36	GENIC	homozygous	59420880
2	226543546	226543547	C	G	27	GENIC	homozygous	59420882
2	226543547	226543548	A	C	27	GENIC	homozygous	59420883
2	226544789	226544790	A	T	37	GENIC	homozygous	59420885
2	226544984	226544985	A	G	16	GENIC	homozygous	59420887
2	226547208	226547209	A	T	18	GENIC	homozygous	59420891
2	226547776	226547777	T	G	28	GENIC	homozygous	59420893
2	226548103	226548104	G	A	24	GENIC	homozygous	59420894
2	226548347	226548348	A	G	20	GENIC	homozygous	59420898
2	226548721	226548725	TGTT	----	12	GENIC	homozygous	60245532
2	226548768	226548769	A	-	22	GENIC	homozygous	59420902
2	226541517	226541518	T	A	25	GENIC	homozygous	60593514