chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39879224	39879225	A	C	11	GENIC	homozygous	126684642
8	39879872	39879873	C	T	10	GENIC	homozygous	126684643
8	39879985	39879986	T	C	6	GENIC	homozygous	126684644
8	39880617	39880618	G	A	17	GENIC	homozygous	126684645
8	39880643	39880644	A	G	22	GENIC	homozygous	126684646
8	39881569	39881570	A	G	18	GENIC	homozygous	126664309
8	39881838	39881839	G	A	21	GENIC	homozygous	126684647
8	39881919	39881920	T	G	16	GENIC	homozygous	126684648
8	39882195	39882196	A	C	12	GENIC	homozygous	126684649
8	39882731	39882732	T	C	6	GENIC	homozygous	126664310
8	39882860	39882861	T	C	9	GENIC	homozygous	126664311
8	39883995	39883996	C	A	11	GENIC	homozygous	126684650
8	39884443	39884444	G	C	18	GENIC	homozygous	126664313
8	39884473	39884474	C	T	17	GENIC	homozygous	126684651
8	39887225	39887226	T	G	20	GENIC	homozygous	126664320
8	39887408	39887409	T	C	21	GENIC	homozygous	126664322
8	39887468	39887469	G	A	13	GENIC	homozygous	126684652
8	39887654	39887655	G	A	10	GENIC	homozygous	126684653
8	39888492	39888493	G	T	16	GENIC	homozygous	126684654
8	39889521	39889522	T	C	12	GENIC	homozygous	116801337
8	39889784	39889785	T	C	13	GENIC	homozygous	116801341
8	39890838	39890839	G	A	11	GENIC	homozygous	116801343
8	39891468	39891469	G	A	6	GENIC	homozygous	116801345
8	39891483	39891484	T	C	7	GENIC	homozygous	116463616