chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	25480722	25480723	T	C	23	GENIC	heterozygous	119485752
18	25480727	25480728	G	C	21	GENIC	possibly homozygous	119485753
18	25480739	25480740	C	G	17	GENIC	heterozygous	119485754
18	25480745	25480746	C	G	16	GENIC	heterozygous	119485755
18	25480775	25480776	C	G	15	GENIC	heterozygous	119485756
18	25480781	25480782	G	C	15	GENIC	heterozygous	119485757
18	25481812	25481813	C	T	50	GENIC	possibly homozygous	110310948
18	25482386	25482387	A	G	59	GENIC	homozygous	110310950
18	25482602	25482603	G	A	22	GENIC	homozygous	119485758
18	25482633	25482634	T	C	22	GENIC	homozygous	110310952
18	25484366	25484367	T	A	24	GENIC	homozygous	119485759
18	25484700	25484701	G	A	35	GENIC	homozygous	110310954
18	25486062	25486063	A	C	77	GENIC	heterozygous	119485760
18	25486076	25486077	G	T	73	GENIC	heterozygous	119485761
18	25486085	25486086	C	T	72	GENIC	heterozygous	119485762
18	25486091	25486092	T	C	80	GENIC	heterozygous	119485763
18	25486101	25486102	C	T	70	GENIC	heterozygous	119485764
18	25486120	25486121	C	A	71	GENIC	heterozygous	119485765
18	25486302	25486303	G	A	57	GENIC	homozygous	110310956
18	25486505	25486506	T	G	33	GENIC	possibly homozygous	119485766
18	25486638	25486639	A	G	33	GENIC	homozygous	119485767
18	25487278	25487279	A	G	34	GENIC	homozygous	110310958
18	25487526	25487527	A	G	42	GENIC	possibly homozygous	110310960
18	25487626	25487627	G	A	47	GENIC	homozygous	110310962
18	25487932	25487933	G	T	29	GENIC	homozygous	110310964
18	25488079	25488080	C	T	39	GENIC	homozygous	110310966