chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	22600776	22600777	T	A	35	GENIC	homozygous	109667601
19	22604980	22604981	T	C	27	GENIC	homozygous	109667603
19	22606812	22606813	A	G	18	GENIC	homozygous	109667605
19	22607950	22607951	C	T	35	GENIC	homozygous	109667607
19	22608012	22608013	C	T	25	GENIC	homozygous	109667609
19	22608900	22608901	A	G	30	GENIC	homozygous	109667611
19	22610279	22610280	G	A	17	GENIC	homozygous	109667613
19	22610314	22610315	T	C	18	GENIC	homozygous	109667615
19	22612051	22612052	A	G	19	GENIC	homozygous	109667617
19	22622591	22622592	A	T	23	GENIC	homozygous	109667619
19	22625719	22625720	A	G	15	GENIC	homozygous	109667621
19	22625953	22625954	C	T	22	GENIC	homozygous	109667623
19	22629764	22629765	T	C	17	GENIC	homozygous	109667627
19	22631562	22631563	G	A	7	GENIC	homozygous	109667629