chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	22599670	22599671	A	C	37	GENIC	heterozygous	119639012
19	22600776	22600777	T	A	69	GENIC	homozygous	109667601
19	22604980	22604981	T	C	67	GENIC	homozygous	109667603
19	22606812	22606813	A	G	53	GENIC	homozygous	109667605
19	22607950	22607951	C	T	46	GENIC	homozygous	109667607
19	22608012	22608013	C	T	55	GENIC	homozygous	109667609
19	22608900	22608901	A	G	54	GENIC	possibly homozygous	109667611
19	22610279	22610280	G	A	68	GENIC	possibly homozygous	109667613
19	22610314	22610315	T	C	66	GENIC	homozygous	109667615
19	22612051	22612052	A	G	66	GENIC	homozygous	109667617
19	22622591	22622592	A	T	44	GENIC	homozygous	109667619
19	22625719	22625720	A	G	48	GENIC	homozygous	109667621
19	22625953	22625954	C	T	47	GENIC	homozygous	109667623
19	22627966	22627967	C	A	67	GENIC	heterozygous	119639013
19	22627980	22627981	T	G	77	GENIC	heterozygous	119601729
19	22629726	22629727	G	T	51	GENIC	homozygous	109667625
19	22629764	22629765	T	C	64	GENIC	homozygous	109667627
19	22631562	22631563	G	A	38	GENIC	homozygous	109667629