chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	100811477	100811478	A	T	18	GENIC	homozygous	108899590
1	100812833	100812834	C	T	38	GENIC	homozygous	108899591
1	100813878	100813879	A	G	10	GENIC	homozygous	108899595
1	100813990	100813991	G	T	18	GENIC	homozygous	108899597
1	100816063	100816064	T	C	24	GENIC	homozygous	108899599
1	100816739	100816740	G	A	14	GENIC	homozygous	108899601
1	100819648	100819649	A	G	20	GENIC	homozygous	108899602
1	100819909	100819910	T	C	21	GENIC	homozygous	108899604
1	100819931	100819932	G	A	15	GENIC	homozygous	108899606
1	100821933	100821934	A	C	20	GENIC	possibly homozygous	108899608
1	100822192	100822193	G	A	30	GENIC	homozygous	108899609
1	100822606	100822607	A	C	21	GENIC	possibly homozygous	108899611
1	100823149	100823150	G	T	24	GENIC	homozygous	108899613
1	100823150	100823151	C	T	24	GENIC	homozygous	108899614
1	100824021	100824022	G	A	27	GENIC	homozygous	108899616
1	100824110	100824111	T	C	42	GENIC	homozygous	108899618
1	100825050	100825051	C	T	20	GENIC	homozygous	108899620
1	100827002	100827003	G	A	25	GENIC	homozygous	108899622