chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	84986503	84986504	A	G	19	GENIC	homozygous	116814732
10	84986553	84986554	C	T	22	GENIC	homozygous	116814736
10	84986693	84986694	C	T	14	GENIC	possibly homozygous	117018696
10	84987790	84987791	T	C	25	GENIC	homozygous	116814738
10	84988740	84988741	G	A	39	GENIC	homozygous	116814740
10	84989258	84989259	C	T	29	GENIC	possibly homozygous	117018697
10	84989502	84989503	A	G	23	GENIC	homozygous	116814742
10	84990335	84990336	G	T	36	GENIC	possibly homozygous	117018698
10	84990523	84990524	G	A	31	GENIC	homozygous	117018699
10	84990828	84990829	T	A	28	GENIC	possibly homozygous	117018700
10	84990829	84990830	C	T	28	GENIC	possibly homozygous	117018701
10	84991703	84991704	G	A	16	GENIC	homozygous	117018702
10	84992273	84992274	A	G	15	GENIC	homozygous	116814754
10	84992329	84992330	A	G	23	GENIC	homozygous	116814756
10	84992420	84992421	T	C	37	GENIC	homozygous	116814758
10	84992677	84992678	G	C	27	GENIC	homozygous	117018703
10	84992987	84992988	T	C	26	GENIC	homozygous	117086809
10	84993118	84993119	G	C	24	GENIC	homozygous	116814760
10	84993210	84993211	T	A	28	GENIC	homozygous	116814762
10	84993377	84993378	G	A	36	GENIC	possibly homozygous	117018704
10	84993915	84993916	T	C	31	GENIC	homozygous	116814764
10	84993981	84993982	G	C	26	GENIC	possibly homozygous	117018705
10	84993999	84994000	T	C	26	GENIC	homozygous	116814766
10	84994072	84994073	T	A	28	GENIC	homozygous	116814768
10	84994100	84994101	C	T	20	GENIC	homozygous	116814770
10	84994219	84994220	A	G	29	GENIC	homozygous	116814772
10	84994230	84994231	T	C	29	GENIC	homozygous	116814774
10	84995051	84995052	C	T	21	GENIC	homozygous	116814776
10	84995488	84995489	A	G	26	GENIC	homozygous	116814778
10	84997028	84997029	G	C	13	GENIC	homozygous	117018706
10	84998181	84998182	G	A	36	GENIC	possibly homozygous	117018707
10	84998487	84998488	A	G	29	GENIC	homozygous	117018708
10	84998850	84998851	A	G	25	GENIC	possibly homozygous	117018709