chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	43616572	43616573	G	A	22	GENIC	homozygous	117171532
10	43616576	43616577	T	C	24	GENIC	homozygous	117171534
10	43616830	43616831	G	A	42	GENIC	homozygous	118081489
10	43616997	43616998	T	C	54	GENIC	possibly homozygous	116578953
10	43617064	43617065	T	G	34	GENIC	homozygous	117171536
10	43617110	43617111	T	G	29	GENIC	homozygous	117171538
10	43617476	43617477	C	G	40	GENIC	homozygous	117171540
10	43617661	43617662	G	A	31	GENIC	homozygous	116578955
10	43618187	43618188	G	T	37	GENIC	homozygous	118081490
10	43618205	43618206	C	T	49	GENIC	homozygous	118081491
10	43618230	43618231	C	G	44	GENIC	homozygous	118081492
10	43618264	43618265	G	A	47	GENIC	possibly homozygous	118081493
10	43618736	43618737	C	A	45	GENIC	homozygous	118081494
10	43618884	43618885	G	C	31	GENIC	homozygous	118081495
10	43619351	43619352	A	G	55	GENIC	homozygous	117171546
10	43619426	43619427	C	G	42	GENIC	homozygous	117171548
10	43619773	43619774	A	G	29	GENIC	possibly homozygous	117171550
10	43620150	43620151	A	G	41	GENIC	homozygous	117171556
10	43620208	43620209	C	G	29	GENIC	homozygous	117171558
10	43620227	43620228	C	A	31	GENIC	possibly homozygous	118081496
10	43620273	43620274	G	A	31	GENIC	homozygous	117171560
10	43620320	43620321	T	C	36	GENIC	homozygous	117171562
10	43620435	43620436	A	C	39	GENIC	homozygous	116578957
10	43620468	43620469	C	T	38	GENIC	homozygous	118081497
10	43620578	43620579	C	A	40	GENIC	homozygous	118081498
10	43620640	43620641	G	A	58	GENIC	possibly homozygous	117171566
10	43619433	43619434	C	T	39	GENIC	homozygous	116766464
10	43620654	43620655	A	G	59	GENIC	heterozygous	117991185