chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	173088032	173088033	G	-	4	GENIC	homozygous	60946949
1	173088039	173088040	G	-	3	GENIC	homozygous	60946951
1	173088278	173088279	G	T	18	GENIC	heterozygous	61961574
1	173089108	173089109	C	T	15	GENIC	homozygous	60946955
1	173089299	173089300	T	C	4	GENIC	homozygous	60946956
1	173090033	173090034	T	C	22	GENIC	homozygous	60946957
1	173090228	173090229	A	G	17	GENIC	possibly homozygous	60946958
1	173090344	173090345	T	C	13	GENIC	possibly homozygous	60946959
1	173091175	173091176	T	G	12	GENIC	homozygous	60946960
1	173091505	173091506	A	G	26	GENIC	possibly homozygous	60946961
1	173091848	173091849	G	A	19	GENIC	possibly homozygous	60946962
1	173094429	173094430	A	AAC	11	GENIC	homozygous	61961575
1	173094449	173094450	C	G	9	GENIC	homozygous	60946963
1	173094519	173094520	T	C	4	GENIC	homozygous	60946966
1	173094612	173094613	C	T	17	GENIC	possibly homozygous	60946967
1	173094632	173094633	A	G	17	GENIC	possibly homozygous	60946968
1	173095238	173095239	A	G	11	GENIC	homozygous	60946969
1	173097074	173097075	G	A	19	GENIC	homozygous	60946972
1	173097323	173097324	C	CA	21	GENIC	homozygous	61961576
1	173097425	173097426	C	A	10	GENIC	heterozygous	60946973
1	173097735	173097739	ACAG	----	10	GENIC	homozygous	60946974
1	173098021	173098022	C	-	14	GENIC	possibly homozygous	60946975
1	173099118	173099119	G	A	19	GENIC	possibly homozygous	61961577
1	173100305	173100306	A	C	8	GENIC	possibly homozygous	62091597
1	173100680	173100681	T	A	27	GENIC	homozygous	60946983
1	173101655	173101656	T	C	26	GENIC	homozygous	61910961
1	173101890	173101891	T	C	25	GENIC	possibly homozygous	61910962