chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	27385458	27385459	G	A	17	GENIC	homozygous	111012998
17	27385767	27385768	T	G	20	GENIC	homozygous	111013000
17	27385820	27385821	A	G	19	GENIC	homozygous	111013002
17	27385926	27385927	G	T	14	GENIC	homozygous	111013004
17	27386011	27386012	T	G	17	GENIC	homozygous	111013006
17	27386238	27386239	G	C	27	GENIC	homozygous	111013008
17	27386294	27386295	A	C	24	GENIC	homozygous	111013010
17	27386295	27386296	A	T	25	GENIC	homozygous	111013012
17	27386499	27386500	T	C	17	GENIC	homozygous	111013014
17	27386518	27386519	T	C	13	GENIC	homozygous	111013016
17	27386727	27386728	G	A	21	GENIC	homozygous	111013018
17	27387622	27387623	T	G	32	GENIC	homozygous	111013022
17	27388516	27388517	C	T	21	GENIC	homozygous	111013024
17	27389045	27389046	A	G	25	GENIC	possibly homozygous	111013026
17	27389046	27389047	A	G	26	GENIC	possibly homozygous	111013028
17	27389298	27389299	G	A	26	GENIC	homozygous	111013030
17	27389341	27389342	G	C	21	GENIC	homozygous	111013032
17	27389613	27389614	T	C	18	GENIC	homozygous	111013034