chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102209417	102209418	T	C	47	GENIC	homozygous	52075576
10	102209669	102209670	T	C	40	GENIC	homozygous	52075578
10	102209679	102209680	G	-	40	GENIC	homozygous	52075580
10	102210043	102210044	A	G	32	GENIC	homozygous	52075582
10	102210407	102210408	C	-	38	GENIC	homozygous	52075584
10	102210741	102210742	G	A	32	GENIC	homozygous	52075586
10	102211238	102211239	G	A	42	GENIC	homozygous	52075588
10	102212116	102212117	G	A	32	GENIC	homozygous	52075590
10	102212733	102212734	G	A	56	GENIC	homozygous	52075592
10	102212860	102212861	G	A	38	GENIC	possibly homozygous	52075594
10	102213584	102213585	T	TG	19	GENIC	homozygous	52075596
10	102213653	102213654	G	-	30	GENIC	homozygous	52075598
10	102213893	102213894	T	-	11	GENIC	heterozygous	51940495
10	102215037	102215038	G	A	34	GENIC	homozygous	52075600
10	102215580	102215581	G	A	33	GENIC	homozygous	52075602
10	102215651	102215652	A	G	34	GENIC	homozygous	52075604
10	102217325	102217329	CAAA	----	18	GENIC	homozygous	52075606
10	102217366	102217367	C	G	28	GENIC	homozygous	52075608
10	102217537	102217538	A	C	32	GENIC	homozygous	52075610
10	102218380	102218381	C	G	29	GENIC	homozygous	52075612
10	102218631	102218632	C	T	35	GENIC	homozygous	52075614
10	102219229	102219230	T	G	24	GENIC	homozygous	52075616
10	102219920	102219921	A	G	34	GENIC	homozygous	52075618