chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53352166	53352167	C	T	13	GENIC	possibly homozygous	59805858
2	53353009	53353010	T	C	29	GENIC	possibly homozygous	58825302
2	53354391	53354392	G	T	23	GENIC	homozygous	59805859
2	53356151	53356152	A	T	13	GENIC	possibly homozygous	58825309
2	53356862	53356863	T	C	4	GENIC	homozygous	58825310
2	53358547	53358548	T	-	14	GENIC	homozygous	58825311
2	53360130	53360131	T	C	6	GENIC	homozygous	59805862
2	53360389	53360390	A	G	21	GENIC	homozygous	58825313
2	53364129	53364130	T	C	18	GENIC	homozygous	58825317
2	53364642	53364643	A	G	16	GENIC	possibly homozygous	59805863
2	53365382	53365383	T	A	23	GENIC	possibly homozygous	58825318
2	53366530	53366531	T	C	22	GENIC	homozygous	59805865
2	53369512	53369513	C	T	26	GENIC	homozygous	58825322
2	53371318	53371319	A	C	6	GENIC	heterozygous	58825324
2	53372009	53372010	C	T	11	GENIC	homozygous	59805866
2	53372033	53372034	T	A	11	GENIC	heterozygous	58825326
2	53373994	53373996	AA	--	2	GENIC	heterozygous	58825327
2	53375587	53375588	T	C	22	GENIC	possibly homozygous	58825330
2	53376683	53376684	T	C	21	GENIC	homozygous	58825332
2	53380073	53380074	T	A	7	GENIC	possibly homozygous	59805868
2	53381318	53381319	C	G	13	GENIC	possibly homozygous	59805870
2	53381778	53381779	T	A	34	GENIC	homozygous	59805871
2	53382393	53382394	C	-	3	GENIC	homozygous	58825343
2	53383247	53383248	G	T	20	GENIC	possibly homozygous	58825345