chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	55062287	55062288	G	GA	8	GENIC	homozygous	46607661
18	55062521	55062522	A	G	19	GENIC	heterozygous	46607662
18	55062644	55062645	C	G	19	GENIC	homozygous	46607663
18	55062665	55062666	T	C	20	GENIC	homozygous	46607664
18	55062895	55062896	A	AAAAAAC	5	GENIC	homozygous	46607666
18	55063508	55063509	T	C	13	GENIC	homozygous	46607667
18	55064051	55064052	G	A	22	GENIC	homozygous	46607668
18	55064846	55064847	G	A	24	GENIC	homozygous	46607669
18	55065435	55065436	C	T	19	GENIC	homozygous	46607671
18	55065495	55065496	G	-	17	GENIC	possibly homozygous	46607672
18	55065578	55065579	A	G	19	GENIC	heterozygous	46607673
18	55066503	55066504	A	G	18	GENIC	homozygous	46463915
18	55066742	55066743	C	T	13	GENIC	possibly homozygous	46607675
18	55067060	55067061	T	C	13	GENIC	homozygous	46607676
18	55067071	55067072	T	C	10	GENIC	homozygous	46607677
18	55067543	55067544	T	C	22	GENIC	possibly homozygous	46607679
18	55068245	55068246	T	G	2	GENIC	homozygous	46607680
18	55068441	55068442	G	A	11	GENIC	homozygous	46607681
18	55068477	55068478	G	A	12	GENIC	homozygous	46607682
18	55069495	55069496	G	A	13	GENIC	heterozygous	46607683
18	55069635	55069636	G	A	13	GENIC	homozygous	46607684
18	55069677	55069678	A	G	4	GENIC	heterozygous	46607685
18	55069820	55069821	A	G	15	GENIC	possibly homozygous	46607686
18	55071012	55071013	C	A	12	GENIC	possibly homozygous	46607692
18	55071139	55071140	A	G	5	GENIC	homozygous	46463921
18	55071193	55071194	C	T	3	GENIC	homozygous	46607693
18	55071680	55071681	T	C	16	GENIC	homozygous	46607694