chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	43616572	43616573	G	A	14	GENIC	homozygous	117171532
10	43616576	43616577	T	C	16	GENIC	homozygous	117171534
10	43616649	43616650	T	C	22	GENIC	homozygous	117007761
10	43616997	43616998	T	C	25	GENIC	homozygous	116578953
10	43617064	43617065	T	G	25	GENIC	homozygous	117171536
10	43617110	43617111	T	G	38	GENIC	homozygous	117171538
10	43617476	43617477	C	G	15	GENIC	homozygous	117171540
10	43617661	43617662	G	A	35	GENIC	homozygous	116578955
10	43618756	43618757	C	T	30	GENIC	homozygous	117171542
10	43618837	43618838	A	G	23	GENIC	homozygous	117171544
10	43619351	43619352	A	G	31	GENIC	homozygous	117171546
10	43619426	43619427	C	G	35	GENIC	homozygous	117171548
10	43619433	43619434	C	T	36	GENIC	homozygous	116766464
10	43619773	43619774	A	G	29	GENIC	homozygous	117171550
10	43619896	43619897	T	A	32	GENIC	homozygous	117171552
10	43620149	43620150	C	T	22	GENIC	homozygous	117171554
10	43620150	43620151	A	G	22	GENIC	homozygous	117171556
10	43620208	43620209	C	G	24	GENIC	homozygous	117171558
10	43620273	43620274	G	A	23	GENIC	homozygous	117171560
10	43620320	43620321	T	C	20	GENIC	homozygous	117171562
10	43620359	43620360	G	C	20	GENIC	homozygous	117171564
10	43620435	43620436	A	C	28	GENIC	homozygous	116578957
10	43620640	43620641	G	A	26	GENIC	homozygous	117171566
10	43620658	43620659	A	T	33	GENIC	homozygous	116578959