chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102209417	102209418	T	C	25	GENIC	possibly homozygous	52075576
10	102209669	102209670	T	C	28	GENIC	possibly homozygous	52075578
10	102209679	102209680	G	-	29	GENIC	possibly homozygous	52075580
10	102210043	102210044	A	G	35	GENIC	homozygous	52075582
10	102210407	102210408	C	-	36	GENIC	homozygous	52075584
10	102210741	102210742	G	A	17	GENIC	homozygous	52075586
10	102211238	102211239	G	A	18	GENIC	homozygous	52075588
10	102212116	102212117	G	A	23	GENIC	homozygous	52075590
10	102212733	102212734	G	A	25	GENIC	homozygous	52075592
10	102212860	102212861	G	A	22	GENIC	homozygous	52075594
10	102213584	102213585	T	TG	25	GENIC	possibly homozygous	52075596
10	102213653	102213654	G	-	22	GENIC	homozygous	52075598
10	102213882	102213883	G	-	6	GENIC	homozygous	52683991
10	102215037	102215038	G	A	31	GENIC	homozygous	52075600
10	102215580	102215581	G	A	27	GENIC	homozygous	52075602
10	102215651	102215652	A	G	24	GENIC	homozygous	52075604
10	102217325	102217329	CAAA	----	14	GENIC	homozygous	52075606
10	102217366	102217367	C	G	23	GENIC	homozygous	52075608
10	102217537	102217538	A	C	37	GENIC	homozygous	52075610
10	102218380	102218381	C	G	35	GENIC	homozygous	52075612
10	102218631	102218632	C	T	35	GENIC	homozygous	52075614
10	102219229	102219230	T	G	23	GENIC	homozygous	52075616
10	102219920	102219921	A	G	37	GENIC	homozygous	52075618