chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	44289860	44289861	A	G	38	GENIC	homozygous	51438700
10	44289891	44289892	C	A	30	GENIC	homozygous	51438701
10	44289894	44289895	T	C	29	GENIC	homozygous	51438702
10	44289899	44289900	C	T	33	GENIC	homozygous	51438703
10	44289932	44289933	T	C	31	GENIC	homozygous	51438704
10	44289936	44289937	C	T	31	GENIC	homozygous	51438705
10	44289939	44289940	G	T	34	GENIC	possibly homozygous	51438706
10	44290024	44290025	T	C	49	GENIC	homozygous	51438707
10	44290055	44290056	A	C	47	GENIC	homozygous	51438708
10	44290149	44290150	A	C	42	GENIC	possibly homozygous	51438709
10	44290214	44290215	G	GGTT	11	GENIC	homozygous	51438710
10	44290274	44290275	C	A	51	GENIC	heterozygous	51438711
10	44290278	44290279	T	A	39	GENIC	homozygous	51438712
10	44290278	44290279	T	C	15	GENIC	homozygous	51438713
10	44290287	44290288	G	T	59	GENIC	heterozygous	51438714
10	44290337	44290338	T	-	47	GENIC	possibly homozygous	51438715
10	44290350	44290351	G	T	65	GENIC	heterozygous	51438716
10	44290367	44290368	A	G	60	GENIC	homozygous	51438717
10	44290440	44290441	T	G	43	GENIC	homozygous	51438718