chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	10550735	10550736	T	TAAA	14	GENIC	possibly homozygous	60626699
1	10552974	10552975	G	GA	18	GENIC	heterozygous	60626700
1	10552974	10552975	G	GAA	18	GENIC	heterozygous	62119642
1	10553467	10553468	T	C	42	GENIC	homozygous	60626701
1	10553904	10553905	G	A	18	GENIC	homozygous	60626702
1	10554178	10554179	A	-	22	GENIC	homozygous	62071695
1	10555373	10555376	AGA	---	24	GENIC	homozygous	60626704
1	10556096	10556097	C	T	24	GENIC	homozygous	60626705
1	10557432	10557433	G	A	28	GENIC	homozygous	60626706
1	10557764	10557765	A	AAAG	19	GENIC	homozygous	60626707
1	10558511	10558512	G	GTT	12	GENIC	heterozygous	62604773
1	10558512	10558513	T	-	12	GENIC	possibly homozygous	60626708
1	10559386	10559387	A	AGT	11	GENIC	heterozygous	62119643
1	10560030	10560031	G	GT	14	GENIC	homozygous	60626709
1	10560612	10560613	G	A	26	GENIC	possibly homozygous	60626710
1	10560615	10560616	G	A	27	GENIC	possibly homozygous	60626711
1	10560665	10560666	T	C	40	GENIC	possibly homozygous	60626712