chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	149142801	149142802	C	A	18	GENIC	possibly homozygous	55787592
5	149142877	149142878	G	A	11	GENIC	homozygous	55787594
5	149142909	149142910	C	T	13	GENIC	homozygous	55787596
5	149142930	149142931	G	A	14	GENIC	homozygous	55787598
5	149143079	149143080	T	C	26	GENIC	possibly homozygous	55787600
5	149143157	149143158	T	C	7	GENIC	homozygous	55787602
5	149143166	149143167	T	-	1	GENIC	homozygous	55787604
5	149143182	149143183	T	C	2	GENIC	homozygous	55787606
5	149143336	149143337	A	G	10	GENIC	homozygous	55787608
5	149143777	149143778	G	T	8	GENIC	possibly homozygous	55787610
5	149144056	149144057	T	C	13	GENIC	possibly homozygous	55787612
5	149144269	149144270	A	AGG	3	GENIC	heterozygous	55787614
5	149144269	149144270	A	AG	3	GENIC	heterozygous	56355995
5	149144276	149144277	A	G	4	GENIC	homozygous	55923748
5	149144649	149144650	G	GGT	13	GENIC	possibly homozygous	55787616
5	149145109	149145110	A	G	3	GENIC	homozygous	55787618
5	149145126	149145127	G	A	4	GENIC	homozygous	55787620
5	149145190	149145191	G	A	9	GENIC	possibly homozygous	55787622