chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	72552093	72552094	A	G	54	GENIC	homozygous	110399151
18	72558961	72558961		TGCTA	13	GENIC	homozygous	129551674
18	72572772	72572772		T	29	GENIC	heterozygous	131209592
18	72575837	72575838	G	T	13	GENIC	homozygous	110399218
18	72587394	72587395	G	T	23	GENIC	possibly homozygous	110498845
18	72599517	72599517		TCTT	34	GENIC	homozygous	129551691
18	72599519	72599519		A	33	GENIC	homozygous	129551692
18	72599520	72599520		TTATT	33	GENIC	homozygous	129551693
18	72599524	72599524		TGGT	35	GENIC	homozygous	129551694
18	72599525	72599525		TTGAGAGTGAGTAGCATATAAAGTTGT	35	GENIC	homozygous	129551695
18	72601027	72601028	G	C	56	GENIC	homozygous	110399274
18	72601226	72601227	A		37	GENIC	homozygous	129551696
18	72601229	72601233	CATT		37	GENIC	homozygous	129551697
18	72601237	72601237		TGGT	38	GENIC	homozygous	129551698
18	72601982	72601983	A	G	31	GENIC	homozygous	119501178
18	72602461	72602461		AAGGA	11	GENIC	homozygous	129551699
18	72602468	72602468		GGGA	8	GENIC	homozygous	129551700
18	72574188	72574189	A	G	65	GENIC	homozygous	110869131
18	72599515	72599516	G	A	34	GENIC	homozygous	110834471